TW200936309A - Electrolitic composite abrasion method and abrasion method - Google Patents

Electrolitic composite abrasion method and abrasion method Download PDF

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Publication number
TW200936309A
TW200936309A TW097138651A TW97138651A TW200936309A TW 200936309 A TW200936309 A TW 200936309A TW 097138651 A TW097138651 A TW 097138651A TW 97138651 A TW97138651 A TW 97138651A TW 200936309 A TW200936309 A TW 200936309A
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Taiwan
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voltage
substrate
polishing
film
conductive film
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TW097138651A
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Chinese (zh)
Inventor
Yasushi Toma
Akira Kodera
Hirokuni Hiyama
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Ebara Corp
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Priority claimed from JP2007264468A external-priority patent/JP2009094343A/en
Priority claimed from JP2007275684A external-priority patent/JP2009102694A/en
Application filed by Ebara Corp filed Critical Ebara Corp
Publication of TW200936309A publication Critical patent/TW200936309A/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23HWORKING OF METAL BY THE ACTION OF A HIGH CONCENTRATION OF ELECTRIC CURRENT ON A WORKPIECE USING AN ELECTRODE WHICH TAKES THE PLACE OF A TOOL; SUCH WORKING COMBINED WITH OTHER FORMS OF WORKING OF METAL
    • B23H5/00Combined machining
    • B23H5/06Electrochemical machining combined with mechanical working, e.g. grinding or honing
    • B23H5/08Electrolytic grinding
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/3205Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
    • H01L21/321After treatment
    • H01L21/32115Planarisation
    • H01L21/3212Planarisation by chemical mechanical polishing [CMP]
    • H01L21/32125Planarisation by chemical mechanical polishing [CMP] by simultaneously passing an electrical current, i.e. electrochemical mechanical polishing, e.g. ECMP

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  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Mechanical Treatment Of Semiconductor (AREA)
  • Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)

Abstract

The present invention provides an electrochemical polishing method capable of increasing a polishing speed while preventing excessive polishing, such as dishing or erosion. In the electrochemical polishing method, when a voltage applied to a conductive film formed on the surface of a substrate is increased at a contact surface pressure of 0 between the surface of the substrate and a polishing pad, a voltage at a first change point C that allows a current density to start to decrease after an increase is referred to as a minimum voltage. In addition, when the voltage is increased at a contact surface pressure having a finite value, a voltage at a second change point B that allows the current density to be maintained constant after the decrease is referred to as a maximum voltage. In this case, the surface of the conductive film is polished while maintaining the voltage to be not lower than the minimum voltage and not higher than the maximum voltage. Further, the present invention provides an electrochemical polishing method capable of rapidly removing a conductive film in regions other than a contact plug or wiring line forming region while preventing excessive polishing, such as dishing or erosion. In the electrochemical polishing method, in a step of increasing a voltage, when the voltage is increased at a contact surface pressure of 0, a voltage at a first change point C that allows a current density to start to decrease after an increase is referred to as a threshold voltage, and the voltage is increased such that a voltage in a region in which a barrier film is exposed is higher than the threshold voltage.

Description

200936309 • 六、發明說明: 【發明所屬之技術領域】 本發明係關於電解複合研磨方法以及研磨方法。 本申請案主張2007年10月10曰提出申請之日本專利 申請案第2007-264468號以及2007年10月23日提出申請 之曰本專利申請案第2007-275684號的優先權,並在此援 用兩個申請案的内容。 【先前技術】200936309 • VI. Description of the invention: [Technical field to which the invention pertains] The present invention relates to an electrolytic composite polishing method and a polishing method. The present application claims priority from Japanese Patent Application No. 2007-264468, filed on Oct. 10, 2007, and the priority of the entire entire entire entire entire entire entire entire entire entire entire entire content The content of the two applications. [Prior Art]

半導體裝置之配線形成製程,一直以來係使用稱為金 屬鑲嵌製程(damascene process),其係在設於絕緣膜内之 溝渠(trench)、通孔(via hole)等的配線用凹部内埋入配 線金屬。此金屬鑲嵌製程,一般而言,係以如下所述之方 式進行:如第6A圖所示,在基板上之由所謂的低介電值 (Low-k)材料等所形成的絕緣膜(層間絕緣膜)62内,形成 「觸插塞(contact plug)或配線形成用的凹部(以下稱為 凹=卩」)63 ’接著在包含凹部肋之層間絕緣膜犯的整 表面形成由氮化鈦等所形成的阻障金屬 膜(以· 為阻障膜」)64,錢在阻障膜64的表面形成由鶴 =形成的金屬導電膜(以下稱為「導電膜」)66,而在凹^ 内埋人金屬導電材料。此時導電膜⑽的表面會形成多 層間絕_62的凹部63相仿之凹部67。然後, 凹部63的外侧之多餘的導電㈣及阻障膜64去除。 =所形成的導電臈66之去除係以化學機 (_方式進行。CMP係如第u圖所示,一邊將研磨聚 320663 4 200936309 w (slurry)52供給至基板W表面的導電膜,一邊將基板W表 面按壓在研磨墊101同時使基板W與研磨墊101相對移 動,而研磨導電膜的表面者(參照例如非專利文獻1,亦即 曰本工業調查會2000年12月出版,土肥俊郎編著之「詳 說半導體CMP技術」第277至284頁)。研磨漿52中含有 磨粒及氧化劑,藉由此氧化劑在第6A圖所示之導電膜66 的表面形成氧化鎢膜。由於形成於導電膜的上段部Η(凹部 67的外侧)之氧化鎢膜會與研磨墊接觸而被去除掉,因此 ❹ 上段部Η的導電膜66會受到研磨。相對於此,形成於導電 膜的下段部L(凹部67的内侧)之氧化鎢膜因不與研磨墊接 觸,故不會被去除掉,於是下段部的導電膜66不會受到研 磨。藉此,使導電膜66的表面的段差(凹部67)消除掉。 為了提高研磨速度,除了供給含有高濃度的磨粒之研 磨漿之外,還必須有高研磨壓力。然而在此情況下,就會 有導電膜的表面容易發生刮痕等之損傷或碟形凹陷 (dishing)(導電膜之過度研磨)之問題。另外,還會研磨到 不應研磨的層間絕緣膜,所以有容易發生磨蝕(erosion) (絕緣膜之過度研磨)之問題。 本發明之第一目的在提供能一種既能防止碟形凹陷及 磨蝕等之過度研磨,且可迅速消除導電膜的表面的段差之 電解複合研磨方法以及研磨方法。此外,雖然有將「電解 複合研磨」看作是「電解研磨」的衍生技術而包含於「電 解研磨」中加以使用之情況,但本說明書仍統一使用「電 解複合研磨」此一用語。另外,此處所謂的電解研磨,係 5 320663 200936309 指利用電解液使導電性物質與對向 電化學作用來加4電性㈣之研磨方;導通,以藉由 述之電化學機械研磨。另外,化學_心在此亦包含後 大型積體電路(LSI)裝置的平坦化(planarizati〇n 配線之層間膜的平坦化)而開發出來之利用工作物血研磨 液的固液反應之濕式的機械化學加工法。電解複合研磨係 利用電解液使導電性物質與對向電極之間導通,以藉由電 化學作用及機械作用來加工導電性物質之研磨方法。 ❹ 另外,本發明之第二目的在提供—種既能防止碟形凹 陷及磨料之過度研磨,又可迅速去除接_塞及配線形 成區域以外的導電膜之電解複合研磨方法。 【發明内容】 本案之發明人發現了以下之事項。亦即,使pH 4至 10之電解液與導電膜接觸然後使施加電壓增加時,電流密 度在預疋的電壓會急遽地變化。使對於導電膜的施加電壓 從0開始增加時,電流密度會與電壓成比例而增加,不過 當電壓超過第一變化點(例如第7圖之A點)之第一變化電 壓而繼續增加時,電流密度會從增加轉而減少。繼而當電 壓超過第二變化點(例如第7圖之B點)之第二變化電壓而 、繼續增加時,電流密度的減少程度會降低,然後電流密度 不再減少而成為大致一定值。此種現象可想成係因為在施 加第一變化電壓以下的電壓時,導電膜的表面形成有對於 電解液而言為溶解性的保護膜,而在施加第二變化電壓以 上的電壓時,導電膜的表面形成有對於電解液而言為不溶 6 320663 200936309 ‘ 性的保護膜之緣故。 已經知道上述之以CMP進行之鎢研磨方法,因為採用 使用pH< 4的酸性研磨漿來形成相當厚的氧化鎢膜,再機 械性地研磨此氧化鎢膜之機制,所以有研磨速度變低之 虞。因此,為了提高研磨速度,而考慮過在供給含有高濃 度的磨粒之研磨漿之外,還使用高研磨壓力來加以因應之 方法,不過已知此方法也會發生問題。 本案之發明人發現,上述的第一及第二變化電壓會依 ❹基板與研磨墊的接觸面壓而變化。接觸面壓愈高,第一及 第二變化電壓愈大,電流密度也愈大。於接觸面壓設為0 之情況施加第一變化電壓(例如第7圖之C點電壓)以下的 電壓時,導電膜的整個表面會形成對於電解液而言為溶解 性的保護膜。另外,於接觸面壓設為有限值之情況施加第 二變化電壓(例如第7圖之B點電壓)以上的電壓時,.導電 膜的整個表面會形成對於電解液而言為不溶性的保護膜。 此等現象,不論導電膜的表面有無段差都一樣。 因此,本發明之一態樣係形成為如下之構成:以在使 前述接觸面壓為0的狀態使前述電壓增加時,電流密度從 增加轉為減少之電壓(例如第7圖之C點電壓)作為最小電 壓,以在使前述接觸面壓為有限值的狀態使前述電壓增加 時,電流密度從增加後減少轉為不再減少之電壓(例如第7 圖之B點電壓)作為最大電壓,而一邊將前述電壓維持在前 述最小電壓以上且前述最大電壓以下,一邊研磨前述導電 膜的表面。 7 320663 200936309 根據此構成,在導電膜的表面有段差之情況,導電膜 與研磨墊的接觸面麼為有限值之上段部(例如第8b圖之上 •kj H) a Ha解性的保護膜,此保護膜會被研磨而完全 去除掉#外,導電膜與研磨塾的接觸面壓為〇之下段部 C例h第8B ®之下段部L)會形成不溶性的保護膜,此保護 膜不會被研磨而殘留下來。藉此,在上段部促進導電膜溶 解到電解液中’在下段部抑制導電膜之溶解。因此,可迅 速消除導電膜表面的段差。 β π 3外、’因為保護膜覆蓋下之下段部的研磨速度相當緩 ,所以導電膜不易發生碟形凹陷之情形。另外,因為藉 由調整施加電壓可抑制上段部的研磨速度,所以可將研磨 塾與導電膜的接觸面壓設定得低些,而可抑制磨鞋。 _另外,本發明之一態樣係形成為如下之構成:以在使 前述接觸面壓為〇的狀態使前述電壓增加時,電流密度從 增加轉為減少之電壓(例如第7圖之c點電壓)作為最小電 ⑩^,以在使刚述接觸面壓為有限值的狀態使前述電壓增加 寸電"IL岔度從増加後減少轉為不再減少之電壓(例如第7 圖之B點電壓)為最大電壓,而一邊將前述電壓維持在前述 最小電壓以上且前述最大電壓以下,一邊研磨導電膜的表 面。 根據此構成,在導電膜的表面有段差之情況,可使導 電膜與研磨塾的接觸面壓為有限值之上段部^列如第8B圖 之上段部H)的電流密度、與接觸面壓為〇之下段部(例如 第8B圖之下段部L)的電流密度之差變大。此電流密度之 320663 8 200936309 ► 差係對應於導電膜之上段部與下段部的研磨速度之差。由 於例如可將電流密度高說成是研磨速度大,因此電流密度 之差大就代表研磨速度之差大。另外,電流密度低係對應 於研磨速度之差小。因此只要適切地控制電流密度的大 小,就能控制研磨速度’所以可迅速消除導電膜表面的段 差。 在本發明之一態樣中’係藉由調整前述電解液之pH而 控制前述導電膜的研磨速度。 © 由於電解液之pH愈大愈促進導電膜之溶解’因此可藉 由調整電解液之pH來控制導電膜的研磨速度。 在本發明之一態樣中,前述電解液係包含會與前述導 電膜反應而生成電氣絕緣性物質之添加劑,且藉由調整前 述添加劑的濃度而控制前述導電膜的研磨速度。 由於前述添加劑的濃度愈大愈會形成強固的保護膜而 不易藉由研磨予以去除,因此可藉由調整前述添加劑的濃 度來控制導電膜的研磨速度。 在本發明之一態樣中,係藉由調整前述研磨墊的轉速 而控制前述導電膜的研磨速度。 由於研磨墊的轉速愈大愈會進行保護膜之去除而促進 導電膜之溶解,因此可藉由調整研磨墊的轉速來控制導電 膜的研磨速度。 本發明之一嘘樣係為具有研磨工序之研磨方法,該研 磨工序係-邊以預定的接觸面壓將基板表面按壓至研磨塾 -邊使前述基板與前述研磨墊㈣移動,而研磨前述基板 320663 9 200936309 表面的導電膜者,該研磨方法的特徵在於:具有以在一邊 使前述基板與前述研磨墊相對移動—邊使前述接觸面麗為 〇的狀態’使電解液與前述導電膜接觸同時施加電壓並使 該電壓增加時,電絲度從增加後減少轉為不再減少之電 壓作為臨限值電壓’ ^在前述研紅序之前,在使前述基 板與前述研磨塾並不接觸之狀態,使電解液與前述導電膜 接觸同時施加前述臨限值電壓以上的電壓,而在前述導電 膜的表面形成保護膜之保護膜形成工序。 根據此構成’藉由在保護膜形成工序中施加臨限值電 的電壓’來形成對於電解液而言為轉性的保護 膜。在接τ㈣研紅序,職科鶴 膜雖會被研磨去除掉,作形成於墓雷腊从 奴Ρ之保濩 烙成於蛤電膜的下段部之保護膜 被研磨而殘留下來。藉此,可迅速消除導電膜表面 的段差。 在本發明之-態樣中,前述研磨工序係為化學機械研 磨工序或電解複合研磨工序。 因為在研磨工序之剛形成保護膜,所以不論是採用化 予機械研磨及電解複合之任—種研磨方法的情況,都 可迅速消除導電膜表面的段差。 本案之發明人發現:藉調整基板表面各部位的電位, 可控制基板各部位的研磨迷度。換言之,形成於基板表面 的金屬膜(亦即下層的錢)與上層的導電狀間存在有電 阻上的差異’利用此差異來調整基板各部位的電位。從設 置於金屬膜的表面之施加點施加電壓至基板表面,在基板 320663 10 200936309 ► 全面都殘存有導電膜之情況,基板的全面會具有大致相等 之電壓。不過,當電壓施加點附近的導電膜被去除而使 膜的一部分露出時,基板表面的電壓分佈就會變化。具- 而言,因為係透過電阻比導電膜高的底膜將電壓施加到= 電膜’所以施加到導電膜的電壓會依與施加點的距離而 低。 降 因此,本發明之一態樣係為藉由一邊使電解液與形成 於基板表面的金屬膜接觸並施加電壓至前述金屬膜,〜 ©以預定的接觸面M將前述基板表面按屋至研磨墊同時使< 述基板與前逑研磨墊相對移動,而研磨前述金屬膜的表别 之電解複合研磨方法,其中,前述電解液係pH 4至1〇者面 前述金屬膜係由下層之底膜及電阻比該底膜小之上層的’ 電膜所構成,該電解複合研磨方法具有:先去除前述電導 -的施加點附近的前述導電膜而使前述底膜露出之工序、壓 及在前述底膜快露出或露出後提高前述電壓之工序,提j ⑩前述電壓:工序,係以在使前述基板與前述研磨墊相對: 動同時使#述接觸面壓為0的狀態提高前述電壓肖,電流 密度從增加轉為減少之電壓作為臨限值電壓,而提高前^ 電壓到使得前述底膜露出區域之電壓超過前述臨限值電 壓。 根據此構成,由於底膜露出區域之電壓超過臨限值電 壓時,電流密度就會轉為減少,因此導電膜的研磨速度會 變低。因此’即使在底膜露出區域有成為接觸插塞或配線 之導電膜存在的情況,也不易在該導電膜的表面形成碟形 11 320663 200936309 凹陷〃另外,因為利用電化學性的溶解作用進行研磨,所 以無需如以往一樣使用高磨粒濃度的研磨製,且無需以高 接觸面壓進行研磨,所以機械研磨作用的比率降低,可防 止磨餘之發生。此外,接觸面壓其有限值係在例如 4 Psi程度。 ^ 參 另一方面’在電阻比底膜小之導電膜仍殘存之區域, 因為施加到導電膜的電壓會依與底膜露出部份的距離 二所以要維持電流密度比底膜露㈣域高之狀態。因此’ ¥電膜殘存之區域,研磨會繼續進行,所以可在抑制刮 痕等之損傷及碟形凹陷的情況下,迅速去除導電^抑則 另外,在本發明之一態樣中,提高前述電壓之工序, 還以士使前述接觸面壓為有限值之狀態提高前述電壓時, 電抓雄度從增加後減少轉為不再減少之電壓作為最大電 屋,而提高前述電壓到使得前述底膜露出區域以外的區域 之電超過前述臨限值麵^在前述最大電独下。 ❿=據此構成’藉由將底膜露出區域以外的區域,亦即 ==存的區域,設定成超過臨限值電麗且在前 將作為接觸SI: 吏件即使在導電膜仍殘存的區域存在有 =為接觸插塞或配線的導電膜之情況,也可維持高電产 .=讀態直到將導電膜研磨到與底_同水平之伟二 該區:坦:在導電膜仍殘存的區域使研磨持續進行而使 膜露出之工序 另外’在本發明之-態财,使前述底 320663 12 200936309 係使前述施加職近邮域t之料基板㈣ 區 前述接觸面壓,構成為比前述施加點附近的區域 域中之前述接觸面壓高。A wiring forming process for a semiconductor device has been conventionally used as a damascene process in which wiring is buried in a wiring recess such as a trench or a via hole provided in an insulating film. metal. This damascene process is generally carried out in the following manner: as shown in FIG. 6A, an insulating film formed of a so-called low dielectric value (Low-k) material or the like on the substrate (interlayer In the insulating film 62, a "contact plug" or a recess for forming a wiring (hereinafter referred to as a recess = 卩) 63' is formed, and then a titanium nitride is formed on the entire surface of the interlayer insulating film including the recess rib. A barrier metal film (which is a barrier film) 64 is formed, and a metal conductive film (hereinafter referred to as "conductive film") 66 formed by the crane is formed on the surface of the barrier film 64, and is recessed. ^ Embedded human metal conductive material. At this time, the surface of the conductive film (10) forms a recess 67 similar to the recess 63 of the plurality of layers. Then, the excess conductive (four) and the barrier film 64 on the outer side of the recess 63 are removed. The removal of the formed conductive crucible 66 is performed by a chemical machine (the CMP system is as shown in Fig. u, while the abrasive poly 320663 4 200936309 w (slurry) 52 is supplied to the conductive film on the surface of the substrate W, The surface of the substrate W is pressed against the polishing pad 101 while the substrate W and the polishing pad 101 are relatively moved, and the surface of the conductive film is polished (see, for example, Non-Patent Document 1, that is, the Sakamoto Industrial Survey, published in December 2000, edited by Toshihiro Jun "Detailed Semiconductor CMP Technology", pp. 277 to 284.) The slurry 52 contains abrasive grains and an oxidizing agent, whereby the oxidizing agent forms a tungsten oxide film on the surface of the conductive film 66 shown in Fig. 6A. The tungsten oxide film of the upper portion of the film (the outer side of the concave portion 67) is removed by contact with the polishing pad, so that the conductive film 66 of the upper portion of the film is polished. On the other hand, the lower portion L of the conductive film is formed. Since the tungsten oxide film (inside of the concave portion 67) is not in contact with the polishing pad, it is not removed, and the conductive film 66 in the lower portion is not subjected to polishing. Thereby, the step of the surface of the conductive film 66 is made (recessed portion 67) ) Eliminated. In order to increase the polishing rate, in addition to supplying a slurry containing a high concentration of abrasive grains, it is necessary to have a high polishing pressure. However, in this case, the surface of the conductive film is liable to be damaged by scratches or the like. (dishing) (over-polishing of the conductive film). In addition, it is also polished to an interlayer insulating film that should not be polished, so that there is a problem that abrasion (over-polishing of the insulating film) is likely to occur. It is an object of the present invention to provide an electrolytic composite polishing method and a polishing method capable of preventing over-polishing of dishing, abrasion, and the like, and rapidly eliminating the surface of the conductive film. Further, although "electrolytic composite grinding" is regarded as The technique of "electrolytic polishing" is included in the "electrolytic polishing". However, the term "electrolytic composite polishing" is used in this specification. In addition, the so-called electrolytic polishing is referred to as 5 320663 200936309. The electrolyte causes the conductive material to interact with the opposite phase to add 4 electric (4) grinding; conduction, by means of electrochemical mechanical research In addition, the chemical_heart also includes the development of a large-scale integrated circuit (LSI) device (the flattening of the interlayer film of the planarizati〇n wiring), which is developed by using the solid-liquid reaction wet of the working blood slurry. The mechanical chemical processing method of the present invention is a polishing method in which an electrolytic solution is used to electrically conduct a conductive substance and a counter electrode to process a conductive substance by electrochemical action and mechanical action. The second object is to provide an electrolytic composite polishing method which can prevent the dishing of the dish and the excessive polishing of the abrasive, and can quickly remove the conductive film outside the connection region of the connection and the wiring. [Invention] The inventor of the present invention found The following matters. That is, when the electrolyte having a pH of 4 to 10 is brought into contact with the electroconductive film and then the applied voltage is increased, the current density is rapidly changed at the pre-existing voltage. When the applied voltage to the conductive film is increased from 0, the current density increases in proportion to the voltage, but when the voltage exceeds the first change voltage of the first change point (for example, point A of FIG. 7) and continues to increase, The current density will decrease from increasing to decreasing. Then, when the voltage exceeds the second change voltage of the second change point (e.g., point B of Fig. 7) and continues to increase, the degree of decrease in current density decreases, and then the current density does not decrease to become a substantially constant value. Such a phenomenon is conceivable because when a voltage lower than the first varying voltage is applied, a surface of the conductive film is formed with a protective film which is soluble for the electrolytic solution, and when a voltage equal to or higher than the second varying voltage is applied, the conductive film is conductive. The surface of the film is formed with a protective film that is insoluble to the electrolyte. The above-described tungsten polishing method by CMP is known, because the use of an acidic slurry of pH < 4 to form a relatively thick tungsten oxide film, and mechanically grinding the mechanism of the tungsten oxide film, the polishing rate becomes low. Hey. Therefore, in order to increase the polishing rate, a method in which a high polishing pressure is applied in addition to a slurry containing a high concentration of abrasive grains is considered, but it is known that this method also causes a problem. The inventors of the present invention have found that the first and second varying voltages described above vary depending on the contact surface pressure of the substrate and the polishing pad. The higher the contact surface pressure, the larger the first and second varying voltages, and the greater the current density. When a voltage equal to or lower than the first varying voltage (e.g., the voltage at point C in Fig. 7) is applied when the contact surface pressure is set to 0, the entire surface of the conductive film forms a protective film which is soluble for the electrolytic solution. Further, when a voltage equal to or higher than a second varying voltage (for example, the voltage at point B in FIG. 7) is applied when the contact surface pressure is set to a finite value, the entire surface of the conductive film forms a protective film which is insoluble to the electrolytic solution. . These phenomena are the same regardless of the surface of the conductive film. Therefore, an aspect of the present invention is configured such that when the voltage is increased in a state where the contact surface pressure is 0, the current density is changed from an increase to a decrease voltage (for example, the voltage at point C in FIG. 7). As the minimum voltage, when the voltage is increased in a state where the contact surface pressure is a finite value, the current density is decreased from the increase to the voltage that is no longer reduced (for example, the voltage at point B in FIG. 7) as the maximum voltage. The surface of the conductive film is polished while maintaining the voltage above the minimum voltage and below the maximum voltage. 7 320663 200936309 According to this configuration, in the case where there is a step on the surface of the conductive film, the contact surface of the conductive film and the polishing pad is a finite upper portion (for example, above the 8b diagram • kj H) a Ha-dissolving protective film , the protective film will be completely removed by grinding #, the contact surface pressure between the conductive film and the polishing crucible is lower than the lower portion C, and the lower portion of the 8B ® lower portion L) forms an insoluble protective film, and the protective film does not Will be ground and left behind. Thereby, the conductive film is promoted to dissolve in the electrolytic solution in the upper portion, and the dissolution of the conductive film is suppressed in the lower portion. Therefore, the step difference of the surface of the conductive film can be quickly eliminated. Outside β π 3 , the polishing speed of the lower portion of the protective film is relatively slow, so that the conductive film is less likely to be dished. Further, since the polishing rate of the upper portion can be suppressed by adjusting the applied voltage, the contact surface pressure between the polishing crucible and the conductive film can be set lower, and the shoe grinding can be suppressed. In addition, an aspect of the present invention is configured such that when the voltage is increased in a state where the contact surface is pressed, the current density is changed from an increase to a decrease voltage (for example, point c in FIG. 7). The voltage is used as the minimum voltage 10^ to increase the voltage increase in the state in which the contact surface pressure is finite, and the IL temperature is reduced from the increase to the voltage that is no longer reduced (for example, FIG. 7B). The point voltage is the maximum voltage, and the surface of the conductive film is polished while maintaining the voltage above the minimum voltage and below the maximum voltage. According to this configuration, in the case where there is a step on the surface of the conductive film, the contact surface of the conductive film and the polishing pad can be pressed to a finite value, and the current density and the contact surface pressure of the upper portion of the segment such as the upper portion H) of FIG. 8B are pressed. The difference in current density between the lower portion (for example, the lower portion L of the eighth drawing) is larger. This current density is 320663 8 200936309 ► The difference corresponds to the difference in the polishing speed between the upper and lower sections of the conductive film. Since the current density is high, for example, the polishing rate is large, the difference in current density is large, which means that the difference in polishing speed is large. Further, the low current density corresponds to a small difference in polishing speed. Therefore, as long as the current density is appropriately controlled, the polishing rate can be controlled so that the step of the surface of the conductive film can be quickly eliminated. In one aspect of the invention, the polishing rate of the foregoing conductive film is controlled by adjusting the pH of the foregoing electrolyte. © Since the pH of the electrolyte increases, the dissolution of the conductive film is promoted. Therefore, the polishing rate of the conductive film can be controlled by adjusting the pH of the electrolyte. In one aspect of the invention, the electrolyte solution contains an additive which reacts with the conductive film to form an electrically insulating substance, and the polishing rate of the conductive film is controlled by adjusting the concentration of the additive. Since the concentration of the aforementioned additive becomes stronger, a strong protective film is formed and is not easily removed by grinding, so that the polishing rate of the conductive film can be controlled by adjusting the concentration of the aforementioned additive. In one aspect of the invention, the polishing rate of the conductive film is controlled by adjusting the rotational speed of the polishing pad. Since the polishing film is removed as the rotation speed of the polishing pad is increased to promote the dissolution of the conductive film, the polishing speed of the conductive film can be controlled by adjusting the rotation speed of the polishing pad. One of the samples of the present invention is a polishing method having a polishing step of polishing the substrate by pressing the substrate surface to a polishing crucible with a predetermined contact surface pressure to move the substrate and the polishing pad (4). 320663 9 200936309 The conductive film on the surface, the polishing method is characterized in that the electrolyte is brought into contact with the conductive film while the substrate is moved relative to the polishing pad while the contact surface is sturdy. When a voltage is applied and the voltage is increased, the wire is decreased from an increase to a voltage which is no longer reduced as a threshold voltage ' ^ before the aforementioned red sequence, the substrate is not in contact with the polishing pad A protective film forming step of forming a protective film on the surface of the conductive film by bringing the electrolytic solution into contact with the conductive film while applying a voltage equal to or higher than the threshold voltage. According to this configuration, a protective film which is conductive to the electrolytic solution is formed by applying a voltage of a threshold voltage in the protective film forming step. In the xi (4) research red order, the medical crane film will be removed by grinding, and the protective film formed in the lower part of the enamel film is formed in the tomb of the tomb wax and is left to be ground. Thereby, the step difference of the surface of the conductive film can be quickly eliminated. In the aspect of the invention, the polishing step is a chemical mechanical polishing step or an electrolytic composite polishing step. Since the protective film is formed immediately after the polishing step, the step of the surface of the conductive film can be quickly eliminated regardless of the case of any of the mechanical polishing and electrolytic polishing methods. The inventors of the present invention found that by adjusting the potential of each part of the surface of the substrate, the polishing unevenness of each part of the substrate can be controlled. In other words, there is a difference in resistance between the metal film formed on the surface of the substrate (i.e., the money of the lower layer) and the conductivity of the upper layer. The difference is used to adjust the potential of each portion of the substrate. A voltage is applied from the application point of the surface of the metal film to the surface of the substrate, and in the case where the substrate is completely covered with a conductive film, the entire substrate will have substantially equal voltages. However, when the conductive film in the vicinity of the voltage application point is removed to expose a part of the film, the voltage distribution on the surface of the substrate changes. In other words, since a voltage is applied to the =electrode film through a base film having a higher electric resistance than the electroconductive film, the voltage applied to the electroconductive film is lower depending on the distance from the application point. Therefore, in one aspect of the present invention, by contacting the electrolyte with a metal film formed on the surface of the substrate and applying a voltage to the metal film, the substrate is ground to a predetermined contact surface M. The electrolytic composite polishing method for polishing the surface of the metal film while the substrate is simultaneously moved relative to the front ruthenium polishing pad, wherein the electrolyte solution is at a pH of 4 to 1 Å, and the metal film is formed by the bottom of the lower layer. The film and the electric resistance are formed by an 'electrode film smaller than the upper layer of the underlayer film, and the electrolytic composite polishing method has a step of removing the conductive film in the vicinity of the application point of the conductance and exposing the underlying film, and pressing and a step of increasing or exposing the base film to increase the voltage, and the step of: increasing the voltage in a state in which the substrate and the polishing pad are opposed to each other while the contact surface pressure is zero. The voltage from the increase to the decrease in the current density is used as the threshold voltage, and the voltage is increased until the voltage of the exposed region of the underlying film exceeds the aforementioned threshold voltage. According to this configuration, since the current density is reduced when the voltage of the exposed portion of the underlayer exceeds the threshold voltage, the polishing rate of the conductive film is lowered. Therefore, even if there is a conductive film which becomes a contact plug or a wiring in the exposed region of the under film, it is difficult to form a dish on the surface of the conductive film. 11 320663 200936309 Depression 〃 In addition, since the electrochemical dissolution is used for the polishing Therefore, it is not necessary to use a polishing system having a high abrasive grain concentration as in the prior art, and it is not necessary to perform polishing at a high contact surface pressure, so that the ratio of the mechanical polishing action is lowered, and the occurrence of abrasion can be prevented. In addition, the contact surface pressure has a finite value such as 4 Psi. ^ On the other hand, 'the area where the resistive film is smaller than the base film remains, because the voltage applied to the conductive film depends on the distance from the exposed portion of the base film, so the current density is higher than the base film exposed (four). State. Therefore, the polishing will continue in the area where the electric film remains, so that it is possible to quickly remove the electric conductivity while suppressing the damage such as scratches and the dishing, and in addition, in one aspect of the present invention, the foregoing is improved. In the process of voltage, when the voltage is increased in a state where the contact surface pressure is a finite value, the electric power is reduced from the increase to the voltage that is no longer reduced as the maximum electricity house, and the voltage is increased to the bottom. The electric power of the area other than the exposed area of the film exceeds the aforementioned threshold surface by the maximum electric power. ❿=According to this, 'the area outside the exposed area of the base film, that is, the area where the == exists, is set to exceed the threshold value and will be used as the contact SI before: even if the conductive film remains There is a case where there is a conductive film which is contact plug or wiring, and high electric power can be maintained. = Read state until the conductive film is ground to the same level as the bottom level. This area: Tan: The conductive film remains. In the region where the polishing is continued to expose the film, in the present invention, the bottom portion 320663 12 200936309 is configured to apply the contact surface pressure of the material substrate (4) region of the application near the postal field t to be The aforementioned contact surface pressure in the region near the aforementioned application point is high.

根據此構成,藉由使施加點料的區財之接觸面 壓,比施加點附近的區域以外的區域中之接觸面高,則 與施加點附近的區域以外的區域相比較,施加點附近的區 域之研磨會受到促進’所以會最先將該區域之導電膜去除 ?。因:b ’可得到在施加點附近處施加於金屬膜的電壓最 咼’隨著與該處的距離增加而電屢降低之電壓分佈。因此, 可在使底膜露出後之提高電㈣王序巾精度良好地去除殘 存的導電膜_。 另外,在本發明之一態樣中,使前述底臈露出之工序, 係使與前述基板相向之對向電極,成為由在同一平面上呈 同心圓狀配置之複數個_小電極所構成之錢電極,且以使 與剛述基板的外側部相向的頻率較高的順序使得研磨速度 較快之方式控制前述分割電極的前述電壓。 根據此構成,藉由以使與前述基板的外側部相向的頻 率較高的順序使得研磨速度較快之方式控制前述分割電極 的電壓,能以從外側部愈向中心部,導電膜的殘存膜厚愈 厚之狀態進行研磨,而確實地使基板周緣部的底膜露出。 另外’在本發明之一態樣中,前述研磨工序,係一邊 以渦電流方式測量前述導電膜的殘存膜厚一邊進行研磨。 根據此構成’藉由以渦電流方式測量導電膜的殘存膜 厚,能進行高精度的膜厚測量。 320663 13 200936309 另外,在本發明之一態樣中,前述導電膜係為鎢膜。 根據此構成,藉由使用鎢膜作為導電膜,使得如上所 述之研磨速度的調整變得容易。 另外,本發明之一態樣係為藉由一邊使電解液與形成 於基板表面的金屬膜接觸並施加電壓至前述金屬臈,一邊 以預疋的接觸面壓將前述基板表面按壓至研磨墊同時使前 述基板與前述研磨墊相對移動,而研磨前述金屬膜的表面 之電解複合研磨方法,其中,前述電解液係pH4至1〇者, ©剛述金屬膜係由下層之底膜及電阻比該底膜小之上層的導 電膜所構成,該電解複合研磨方法具有:將前述電壓之施 加點配置於前述基板的周緣部而先去除周緣部的前述導電 膜使前述底膜露出之工序、以及在該工序之後使前述電壓 之施加點從基板的周緣部向中心部移動而使前述底膜露出 之工序。 根據此構成,藉由在使底膜露出後,使電壓之施加點 ⑩從基板的周緣部向中心部移動,可使底祺露出區域的電壓 維持在較高的狀態。藉此,即使在底膜露出區域有將成為 接觸插塞或配線之導電膜存在的情況,也不易在該導電膜 的表面形成碟形凹陷。 另外,本發明之一態樣係為藉由一邊使電解液與形成 於基板表面的金屬膜接觸並施加電壓至前述金屬膜,一邊 以預定的接觸面壓將前述基板表面按壓至研磨墊同時使前 述基板與前述研磨墊相對移動,而研磨前碟金屬膜的表面 之電解複合研磨方法,其中,前述電解液係邱4至1〇者, 320663 14 200936309 * 前述金屬臈係由下層之底膜及電阻比該底膜小之上層的導 電膜所構成,該電解複合研磨方法具有:將前述電壓之施 加點配置於前述基板的周緣部而先去除該周緣部的前述導 電膜使前述底膜露出之工序、在該工序之後使前述電壓之 施加點從前述基板的周緣部向中心部移動而使前述底膜露 出之工序、以及在前述底膜快露出或露出後提高前述電壓 之工序,提高前述電壓之工序,係以在使前述基板與前述 研磨墊相對移動同時使前述接觸面壓為0的狀態提高前述 © 電壓時,電流密度從增加轉為減少之電壓作為臨限值電 壓,而提高前述電壓到使得前述底膜露出區域之電壓超過 前述臨限值電壓。 根據此構成,藉由使電壓之施加點從基板的周緣部向 中心部移動,則即使未使電壓大幅上升,也可使底膜露出 區域的電壓在臨限值電壓以上。藉此’即使在底膜露出區 域存在有將成為接觸插塞或配線之導電膜的情況,也不易 Φ在該導電膜的表面形成碟形凹陷。 【實施方式】 以下參照圖式詳細說明本發明之一個以上的實施形 態。 (基板處理裝置) 第1圖係顯示具備有本發明相關的電解複合研磨裝置 之基板處理裝置的配置構成之平面圖。此基板處理裝置3〇〇 具備有收容基板匣204之裝载/卸載台(1〇ad/unl〇ad stage) ’基板匣204中可儲存多數個基板讯。走行機構2〇〇 15 320663 200936309 之上配置有具有兩個機器年劈 飛裔于質之搬送機器人202,以使搬 =器人202可到達裝載/卸載台内之各基板㈣4。走行 採用由線性馬達所構成之走行機構。藉由採用 由線性馬達所構成之走行機構,即使是大口徑化且重量辦 加=基板’例如具有450咖直徑㈣晶圓,也可進行高i 且穩定之搬送。在走行機構_的延長線上,配置有在研 磨則或研磨後進行基板上的膜厚測量之πΜ,亦即在線厚 度監測器(In-line Thickness Monit〇r)224。According to this configuration, when the contact surface pressure of the spot material to be applied is higher than the contact surface in the region other than the region near the application point, the vicinity of the application point is compared with the region other than the region near the application point. The grinding of the area will be promoted' so the conductive film of the area will be removed first. Since b' can obtain a voltage distribution which is applied to the metal film at the vicinity of the application point, the voltage 屡' decreases as the distance from the portion increases. Therefore, it is possible to remove the remaining conductive film _ with high precision after the base film is exposed. Further, in one aspect of the invention, the step of exposing the bottom rim is such that the counter electrode facing the substrate is composed of a plurality of _ small electrodes arranged concentrically on the same plane. The money electrode is controlled to control the voltage of the divided electrode in such a manner that the frequency of the outer surface of the substrate is higher than the outer portion of the substrate. According to this configuration, by controlling the voltage of the divided electrode so that the polishing rate is faster in a procedure in which the frequency toward the outer portion of the substrate is higher, the residual film of the conductive film can be made from the outer portion toward the center portion. The thicker and thicker state is polished, and the base film of the peripheral portion of the substrate is surely exposed. Further, in one aspect of the invention, the polishing step is performed while measuring the residual film thickness of the conductive film by an eddy current method. According to this configuration, by measuring the residual film thickness of the conductive film by the eddy current method, it is possible to perform film thickness measurement with high precision. 320663 13 200936309 Further, in one aspect of the invention, the conductive film is a tungsten film. According to this configuration, by using the tungsten film as the conductive film, the adjustment of the polishing rate as described above is facilitated. Further, an aspect of the present invention is to press the surface of the substrate to the polishing pad with a pre-twisted contact surface pressure while bringing the electrolytic solution into contact with the metal film formed on the surface of the substrate and applying a voltage to the metal crucible. An electrolytic composite polishing method for polishing the surface of the metal film by moving the substrate and the polishing pad, wherein the electrolyte solution is pH 4 to 1 Å, and the metal film is composed of a lower layer and a resistor. The electroconductive composite polishing method includes a step of arranging the application point of the voltage on a peripheral portion of the substrate, and removing the conductive film on the peripheral portion to expose the underlayer, and After this step, the step of applying the voltage is moved from the peripheral edge portion of the substrate to the central portion to expose the underlayer film. According to this configuration, after the base film is exposed, the voltage application point 10 is moved from the peripheral edge portion of the substrate to the center portion, whereby the voltage in the bottom exposed region can be maintained at a high level. Thereby, even in the case where the conductive film to be contact plug or wiring exists in the exposed region of the under film, it is difficult to form a dish-shaped recess on the surface of the conductive film. Further, an aspect of the present invention is to press the surface of the substrate to a polishing pad with a predetermined contact surface pressure while bringing the electrolytic solution into contact with the metal film formed on the surface of the substrate and applying a voltage to the metal film. An electrolytic composite polishing method for moving the surface of the metal film before polishing, and the surface of the metal film before polishing, wherein the electrolyte solution is 4 to 1 ,, 320663 14 200936309 * the metal lanthanum is a bottom film of the lower layer and a conductive film having a lower electric resistance than the base film, wherein the electrolytic composite polishing method has a step of disposing the voltage applied to a peripheral portion of the substrate, and first removing the conductive film on the peripheral portion to expose the base film a step of moving the voltage application point from the peripheral edge portion of the substrate to the center portion after the step to expose the base film, and a step of increasing the voltage after the base film is exposed or exposed, thereby increasing the voltage In the step of moving the substrate and the polishing pad relative to each other, the contact surface pressure is increased to zero. © When the voltage is applied, the current density changes from increasing to decreasing as the threshold voltage, and the voltage is raised to such a value that the exposed area of the underlying film exceeds the threshold voltage. According to this configuration, by moving the voltage application point from the peripheral edge portion of the substrate to the center portion, the voltage in the exposed portion of the base film can be equal to or higher than the threshold voltage even if the voltage is not largely increased. Therefore, even if a conductive film which will become a contact plug or a wiring exists in the exposed region of the under film, it is difficult to form a dish-shaped recess on the surface of the conductive film. [Embodiment] Hereinafter, one or more embodiments of the present invention will be described in detail with reference to the drawings. (Substrate Processing Apparatus) Fig. 1 is a plan view showing an arrangement configuration of a substrate processing apparatus including an electrolytic composite polishing apparatus according to the present invention. The substrate processing apparatus 3 is provided with a loading/unloading stage (1〇ad/unl〇ad stage) in which the substrate 匣 204 is accommodated. A plurality of substrate signals can be stored in the substrate 匣 204. The traveling mechanism 2 〇〇 15 320663 200936309 is provided with a transport robot 202 having two machine-aged flying bodies, so that the transporter 202 can reach the substrates (4) 4 in the loading/unloading station. Traveling The traveling mechanism consisting of a linear motor is used. By using a running mechanism composed of a linear motor, even if the diameter is large and the weight of the substrate is, for example, 450 wafer diameter (four) wafers, high-yield and stable conveyance can be performed. On the extension line of the running mechanism _, there is disposed π Μ which is a film thickness measurement on the substrate after grinding or polishing, that is, an in-line thickness monitor (In-line Thickness Monit〇r) 224.

隔著搬送機器人202的走行機構綱而與 相對的-侧配置有兩台錢單元2仏各觀單元212係 配置在搬送機器人202之機器手臂可到達的位置。另外在 兩台乾燥單兀212之間’在搬送機器人2()2可到達的位置 配置有具備四個基板載置台之基板站。 在可到達各乾燥單元212與基板站206之位置,配置 有搬送機器人208。在搬送機器人208之機器手臂可到達 的位置配置有與乾燥單元212鄰接之洗淨單元214。在搬 送機器人2G8之機器手臂可到達的位置配置有旋轉輸送器 210’且在可與此旋轉輸送器21〇進行基板的傳送接收之位 置,配置有兩台本實施形態之電解複合研磨裝置25〇。 各電解複合研磨裝置250具有:基板頭1、研磨台1〇〇、 研磨墊101(參照第2圖等)、將電解液供給至研磨墊1〇1 之電解液供給喷嘴(電解液供給部)1〇2、用來進行研磨墊 101的修整(dressing)之修整器218、以及為了洗淨修整器 218而設之水槽222。 . 16 320663 200936309 (電解複合研磨裝置) 2圖^干二 研磨^ 250之概略構成圖。如第 =Λ:1係透過萬向接頭部1〇而連接至基板頭 =基f頭驅動轴11係連結至基板頭用氣紅m, :=二U1固定至襬動臂110。基板頭驅動軸η 藉由基板頭用乳紅111而卜 C2泠脾151宁认苴α 下移動,使基板頭1整體升降, 以及將固疋於基板頭本體2的下端之扣環(恤^咖) Ο 3按壓至研磨台議。基板氣幻u係透過調節器 (regulatoiOREl而連接至壓縮空氣源12〇,藉由調節器rei 可調整供給至基板頭用氣缸1U之加壓空氣的氣壓等之流 體壓力。藉此,可調整扣環3按壓研磨墊ιοί之按壓力。 基板頭驅動軸11係透過鍵(key)(未圖示)而連結至旋 轉筒112。旋轉筒112的外周部具備有時規滑輪(timing pulley)113。擺動臂110固定有作為旋轉驅動部之基板頭 用馬達114,且時規滑輪113透過時規皮帶115而與設在 基板頭用馬達114之時規滑輪jig連接。因此,驅使基板 頭用馬達114轉動,在時規滑輪116、時規皮帶115及時 規滑輪113的傳動下’旋轉筒112及基板頭驅動軸11就會 一體轉動,而使基板頭1轉動。擺動臂110係由固定且支 撐於框架之軸117加以支撐、 (基板頭) 第3圖係顯示基板頭1之斷面圖,第4圖係第3圖所 示之基板頭1的底面圖。如第3圖所示,基板頭1具備有: 内部具有收容空間之圓筒容器狀的基板頭本體2、以及固 17 320663 200936309 - 定於基板頭本體2的下端之扣環3。基板頭本體2係由例 如金屬、陶瓷等之高強度及剛性的材料所形成。扣環3係 由例如PPS(聚苯硫醚;polyphenylene sulfide)等之高剛 性的樹脂或陶瓷等之絕緣材料所形成。 基板頭本體2具備有圓筒容器狀的殼體部2a、嵌合於 殼體部2a的圓筒部的内侧之環狀的加壓片支持部2b、及 散合於殼體部2a的上表面的外周緣部之環狀的密封部 2c。固定於基板頭本體2的殼體部2a的下面之扣環3的下 ❹部係向内侧突出。此外,扣環3與基板頭本體2亦可一體 形成 基板頭本體2的殼體部2a的中央部上方配設有上述基 板頭驅動軸11,基板頭本體2與基板頭驅動軸u係藉由 萬向接頭部10而連結。此萬向接頭部1〇具備有使基板頭 本體2與基板頭驅動軸u可相互傾斜運動之球面軸承機 構、及將基板__ U之婦傳遞至基板頭本體2之旋 轉傳遞機構’以在容許基板頭讀2相對於基板頭驅動軸 之4員斜運動的同_,將基板頭驅動軸Η的按壓力及旋 轉力傳遞至基板頭本體2。 士球面轴承機構係由形成於基板頭驅動軸11的下表面 央之球面狀凹部lla、形成於殼體部^的上表面中央3 灸',狀凹部2d、以及安裝在兩凹部Ua,2d之間並由陶旁 硬度材料所形成之軸承球12所構成。旋轉傳遞名 於二辦固定於基板頭驅動轴11之驅動銷(未圖示)及固定 體部%之被驅_肖(未麻)職成。因為即使基㈣ 320663 18 200936309 • 本體2傾斜,被驅動銷及驅動銷也可相對地朝上下方向移 動,所以兩凹部及軸承球相互的接觸點雖會偏移但 合’旋轉傳遞機構可確實地將基板頭驅動軸n的轉矩傳遞 至基板頭本體2。 基板頭本體2及一體固定於基板頭本體2之扣環3的 内部所區隔形成的空間内,收容有:與基板頭保持的 半導體晶圓等的基板W抵接之彈性墊4、環狀的保持環5、 及支持彈性塾4之約略為圓盤狀之爽持板(咖咖叩山⑹ β 6。彈性塾4的外周部係夾在保持環5與固定於該保持環5 的下端之夾持板6之間,將夾持板6的下面覆蓋住。藉此, 在彈性墊4與夾持板6之間形成空間。 保持環5與基板頭本體2之間設有張開之由彈性膜所 形成之加壓片7。加壓片7係由例如三元乙丙橡膠 (Ethylene-Propylene Diene Monomer rubber : EPDM)、聚 胺酯橡膠(p〇lyUrethane rubber)、矽橡膠(siUc〇nrubber) ❹等之強度及耐久性良好之橡膠材所形成。加壓片7係使其 一端夾於基板頭本體2之殼體部2a與加壓片支持部2b之 間、另一端夾於保持環5之上端部5a與擋止部5b之間而 得以固定。藉由基板頭本體2、夾持板6、保持環5及加壓 片'在基板頭本體2的内部形成壓力室21。如第2圖所示, 由管子及接頭等所構成之流路31從壓力室21開始延伸設 置,壓力室21通過設於流路31内之調節器RE2而與壓縮 空氣源120連接。 此外,第3圖所示之加壓片7由橡膠等的彈性體所形 19 320663 200936309 成,且將加壓片7夾在扣環3及基板頭本體2之間而加以 固定時,扣環3的下表面會因為本身屬於彈性體之加壓片 7的彈性變形而無法得到想要的平面。因此,為了防止這 種情形’在本例中另外設置加壓片支持部2b此一構件,將 加壓片7夾在基板頭本體2之殼體部2a與加壓片支持部 2b之間而加以固定。 形成於彈性墊4與夾持板6之間的空間的内部,設有 作為與彈性墊4抵接的抵接構件之中央袋(中心部抵接構 ❹件)8、及環形管(外側抵接構件)9。在本例中,如第3及第 4圖所示,中央袋8係配置在夾持板6的下面的中心部, 環形管9係以圍在中央袋8的周圍之方式配置在中央袋8 的外侧。此外彈性墊4、中央袋8及環形管9係與加壓片7 —樣由例如三元乙丙橡膠(EPDM)、聚胺酯橡膠、矽橡膠等 之強度及耐久性良好之橡膠材所形成。 如第3圖所示,形成於夾持板6及彈性墊4之間的空 e 間在上述中央袋8及環形管9的區隔下形成複數個空間, 在中央袋8及環形管9之間形成壓力室22 ,在環形管9的 外側形成壓力室23。 中央袋8係由與彈性墊4的上表面抵接之彈性膜81、 ^以可裝拆的方式保持彈性膜81之中央袋保持件(保持 邛)82所構成。中央袋保持件82形成有螺絲孔,將螺 ^ 55鎖接到該螺絲孔孤,就可將中央袋8 =裝到錄板6的下表面財,_。中錄8的=藉方 彈度膜81及中央袋保持件82而形成有中心部壓力室冰 20 320663 200936309 同樣地’環形管9係由與彈性墊4的上表面抵接之强 性膜9卜及以可裝拆的方式保持彈性膜91之環 件(保持部)㈣構形管保持件92形成有螺絲孔 92a ’將螺絲56鎖接到該螺絲孔㈣,就可將環形管 可裝拆的方式安裝戯持板6的下表面。環形管9的 藉由彈性膜91及環形管保持件92而形成有中間部壓力^ 25 〇 壓力室22,23、中心部壓力室24及中間部壓力室^ ©分別與由管子及接頭等所構成之流路從% %,%相連 通,各壓力室22至25通過設於各流路33至%内之調節 器㈣,聰,RE5,廳而與作為供給源之壓縮空氣源12〇 連接。此外’上述流路31、33至36係透過設於基板頭驅 動軸11 #上端部之旋轉接頭(未圖示)而連接至各調節器 RE2 至 RE6。 於是加壓空氣等之加壓流體等經由與各聲力室連通之 ❹机路31、33至36而供給至上述之夾持板6的上方的壓力 室21以及上述壓力室22至25。如第2圖所示,藉由配置 在壓力至21至25的流路31、33至36上之調節器RE2至 腿,可調整供給至各個壓力室之加壓流體的壓力。藉此就 可分別獨立控制各壓力室21至25的内部的壓力,或者使 各壓力至21至25的内部為大氣壓或真空。 如此,藉由調節器RE2至RE6使各壓力室21至25的 内部的壓力可獨立變化,就可針對基板w的各個#份(劃分 區域)凋整透過彈性墊將基板ψ按壓至研磨墊“I之按壓 320663 200936309 力。 另外如第3圖所示,從夾持板6向著壓力室22,23立 设有複數個凸部42。凸部42的前端通過開口部41而露出 到彈性墊4的表面。另外’設置有從凸部42的前端面開始 延伸之流路43,此流路43連接至第2圖所示之真空源 121。藉此’就可用第3圖所示之凸部42的前端面以真空 吸力將基板W吸起。 如第2圖所示,電解複合研磨裝置250的研磨台1〇〇 © 中埋設有測量基板表面的導電膜等的膜厚之由例如渦電流 感測器所構成之ITM 226的感測器線圈228。此ITM 226 輸出的訊號係輸入至控制部310,此控制部310的輸出用 來控制調節器RE3至RE6。 (研磨台、研磨塾) 第5A圖·係概略地顯示電解複合研磨裝置的..重要部份 之縱斷面圖。研磨台100的上面固定有圓板狀的支持構件 ❹ 254。支持構件254係以導電性材料(金屬、合金、導電性 塑膠等)構成。此支持構件254的上面安裝有研磨墊101, 研磨墊101的上表面成為研磨面。研磨台1〇〇連結至未圖 示的旋轉機構,研磨台100藉此而能與支持構件254及研 磨墊101 —體旋轉。 電解液供給噴嘴102係沿著研磨墊1〇1的半徑方向延 伸。電解液供給噴嘴102的前端設有電解液的供給口 l〇2a。此供給口 102a位於研磨墊ιοί的中央部的上方,電 解液從未圖示的電解液供給源通過電解液供給喷嘴1〇2而 22 320663 200936309 供給到研磨塾1G1的中央部。當研磨墊1G1旋轉時,電解 液會向外_散潤濕,且充填於基板頭 1及研磨墊101之 間以及研磨塾1Q1的複數個貫通孔lGla之中。 支持構件254與電源252的負極連接,具有第—電極 (丢極)之功能。從電源252延伸出來的配線與支持構件(陰 極254的電氣接點係採用滾子(roller)、電刷(brush)等。 例如,如筮q A固β - ❹ Α圖所不,可使電氣接點262與支持構件254 、i面接觸。電氣接點262較佳為以比電阻小的軟質金 屬心】如金、銀、網、白金、把等來形成。 位在研磨墊101侧邊’配置有與電源252的正極連接 w沾一 a極(°電電極或施加點)264。基板頭1係以讓基板 、刀在研磨塾101的側邊露出之狀態使基板W與研 面接觸’使基板W的下表面會與第二電極264接觸。藉 從第/電極264供電至基板。另外,』 作而從第二電極264供電至基板?的導電膜。於是, 支持構件254與作為陽極之基板w上的導電膜 接。°、,磨塾101的貫通孔101a中之電解液而電性連 Iί 5B圖係概略地顯示電解複合研磨裝置的其他的重 254其太ρΓΓ 解複合研磨装置250的支持構件 板狀的底件咖、及覆蓋在此底件· 的上面之蓋件254a所構成。如上 作為陰極(第一雷搞a 叉符構仵“4具有 之至少j ,所以蓋件254a及底件254b 夕方要由導電性材料所構成。 320663 23 200936309 支持構件254之蓋件恥在與研磨塾ι〇ι的上述貫通 孔101a相同的位置形成有複數個連通孔255。另外,在蓋 件254a的下表面形成有與該等連通孔挪相連通之複數個 連通溝256。此外’亦可在底件254b的上表面設置連通溝。 研磨塾101的中央部,形成有上下貫通研磨墊1()1之第一 電解液接受口 258A1外,在蓋件254a之與第—電解液 接夂口 258A相同的位置形成有第二電解液接受口 25犯。 第二電解液接受口 258B與上述複數個連通溝256相連通。 藉由如此之構成’從電解液供給喷嘴1〇2的供給口 102a供給來的電解液,會依序流過第一電解液接受口 258A、第二電解液接受口 258B、連通溝256及連通孔255 而到達貫通孔101a。然後,在貫通孔1〇la的内部形成向 著研磨面之電解液的向上流動,而將電解液供給到研磨面。 (第一實施形態、電解複合研磨方法)._ 接著,針對第一實施形態之電解複合研磨方法進行說 明。 第6A圖係研磨前的基板之說明圖。首先,針對屬於本 實施形態的研磨對象之基板W的膜構成進行說明。在由矽 等所形成之基板W的表面,形成有由所謂的低介電值 (Low-k)材料、或siCh,SiOF,SiOC等的絕緣材料所形成 的層間絕緣膜62。層間絕緣膜62的表面,形成有接觸插 塞或配線形成用的凹部63。在包含此凹部63在内之層間 絕緣膜62的表面,形成有厚度在nm程度之由鈦、粗、 鎢、釕及/或此等金屬的合金等所形成的阻障膜64。陴障 24 320663 200936309 1 膜64係為了防止後述之導電膜66的金屬材料擴散到基板 W,或為了提高導電膜66與層間絕緣膜62的密著性而設 置。阻障膜64的表面形成有厚度在500至600 nm程度之 由鎢所形成的導電膜66。使用電解鍍覆法來形成此導電膜 66時,會在阻障膜64的表面先形成作為電解鍍覆的電極 之種子膜(未圖示)。導電膜66的表面會形成與層間絕緣膜 62的凹部63相仿之高度在300 nm程度、寬度在100 /zm 程度之凹部67。另外,亦可用鎢以外之鋁、銅、銀、金或 © 此等金屬的合金等導電性金屬材料來形成導電膜66。 因為只有充填於層間絕緣膜62的凹部63内的導電膜 66會利用作為接觸插塞或金屬配線,所以並不需要形成於 凹部63的外侧之導電膜66。因此,藉由電解複合研磨將 多餘的導電膜66去除。 第6B圖係電解複合研磨之說明圖。電解複合研磨係一 邊使電解液50與基板W表面的導電膜接觸並施加電壓至導 電膜66,一邊將基板W表面按壓至研磨墊101同時使基板 W與研磨墊101相對(旋轉)移動,而研磨導電膜66的表面 者。 因為要隔著層間絕緣膜層疊形成複數條配線,所以有 必要以將多餘的導電膜66去除掉的狀態使基板W的表面平 坦化。電解複合研磨就是藉由施加電壓至導電膜66,在導 電膜66的表面形成由電氣絕緣性物質所形成之保護膜 70。形成於導電膜66的上段部Η(凹部67的外侧)之保護 膜會與研磨墊101抵觸而被去除掉。因此,上段部Η的導 25 320663 200936309 電膜66會溶解於電解液50而被去除掉。相對於此,下段 部L(凹部67的内侧)之導電膜則為保護膜7〇所遮蔽而不 會溶解於電解液50。藉由以上之電解複合研磨,使導電膜 的段差消除掉。藉此,如第6C圖所示,讓導電膜66的表 面與露出的阻障膜64的表面配置在同一平面上,而使基板 W平坦化。 然而’以CMP進行之鎢研磨方法,因為採用使用pH< 4的酸性研磨漿來形成相當厚的氧化鎢膜,再機械性地研 © 磨此氧化鎮臈之機制,所以有研磨速度變低之處β因此, 本實施形態之電解複合研磨方法採用ρΗ 4至10之電解 液,來形成與以往的氧化鎢膜不同之保護滕。此處,係在 加工開始時採用PH在4至1〇的範圍内之電解液。不過, 因為加工時產生之氫等的緣故,所以加工開始進行之後, 電解液的pH就可能會變化β因此,所謂電解液的pH值在4 至10的範圍内,係至少加工開始前、加工中、或加工結束 ❿時之pH會落在4至10的範圍内,另外在實質進行加工之 際pH也會落在該範圍内。邱值之測量係採用H〇RIBA公司 製造的pH測量器D51S(手持式),且有加上溫度修正,並 採用玻璃電極法(JIS形式1)。測量係在2〇°c至30°c之大 致室溫下進行。 此外,在本實施形態中,只要具有適當的導電率 (lmS/cm程度),基本上任何電解液都可使用。電解液中所 含的主電解質,則只要能提供適當的導電率,且不會使導 電膜的表面變粗键者皆可。而且,以會與鎢形成錯合物或 26 320663 200936309 螯合物’且會促賴的轉者為佳,且以包含例如有機酸 為佳。有機酸以使用從乙醇酸、焦鱗酸、構酸、捧檬酸、 韻果酸、順丁烯二酸、丙二酸、乳酸、酒石酸、破拍酸、 及此等酸的鹽所組成的群組中選擇之任一種或複數種為 佳pH之範目α #易生成鱗為溶解性的化合物之錯合物 或螯合物之pH 4至10為佳。 電解液中亦可含有pH簡成分。p請㈣分可使用 鹼金屬鹽、鹼土金屬鹽等,但為了防止金屬污染以銨鹽為 ❹佳。 電解液中亦可含有會生成電氣絕緣性物質之添加劑。 會生成電氣絕緣性物質之添加劑可利用一級胺聚合物,例 如烯丙胺聚合物(侧鏈只具有一級胺基之聚合物,分子量 1,000至60,000)、烯丙胺鹽酸鹽聚合物(分子量1 000至 60’ 000)、烯丙胺鹽酸.鹽-二烯丙胺鹽酸鹽共聚物(分子量.· 20,000至1〇〇,〇〇〇)、烯丙胺氨基磺酸鹽聚合物(分子量 ❹I2, 000)、烯丙胺醋酸鹽-二烯丙胺醋酸鹽共聚物(分子量 100, 000)、烯丙胺-二甲基烯丙胺共聚物(分子量丨,〇〇〇)、 邛为甲基羰基化烯丙胺聚合物(分子量15,000)、部分甲基 羰基化烯丙胺醋酸鹽聚合物(分子量15,000)等。另外,一 級胺聚合物亦可為聚乙亞胺(分子量L _至70, _)。聚 乙亞胺係分子中具有同時包含—級、二級、三級胺的分支 構k之I合物,因為分子内有—級胺所以具有效果。 會生成電氣絕緣性物質之添加劑的較佳的濃度,在聚 乙亞胺的情況為0. 01至5重量%,更佳為〇.工至1重量%, 27 320663 200936309 濃度低於0.01重量%則電流抑制效果(電氣絕緣性)較低, 另一方面,使濃度高於5重量%的情況,因為相對於添加量 的增加之電流抑制效果的增強有降低的傾向,所以沒有使 濃度高到5重量%以上之必要。.藉由添加此種會生成電氣絕 緣性物質之添加劑,可如後述般使段差消除性高的電壓範 圍向低處偏移。 過去,在CMP的情況,磨粒的濃度必須在1〇%以上, 但在本實施形態則即使濃度在1%以下也有很好的效果。此 ❿外’雖然也可添加界面活性劑來提高磨粒的分散性,但因 為磨粒的濃度原本就很低,所以即使不添加也不會有很大 的問題。 舉一個如上述的電解液的例子來說,有本實施形態中 所採用之檸檬酸銨(pH 8)。 “ 關於鎢的研磨速度’本案之發明人用以下說明的方法 進行了實驗、評估。 ❺ 使用可只加工基板之相當於直徑40 mm的部份之電解 研磨裝置進行加工實驗。此裝置係可控制在基板上成膜之 金屬膜的電極電位,且以—邊施加電壓,—邊用黏貼在旋 轉的研磨台上的研磨墊來研磨露出的金屬膜之方式進行加 工。關於實驗結果,舉一個具體的例子來說,每1〇mA/cm2 的電流费度可獲得50至150 nm/min程度之研磨速度。 電極電位之測量係使用電化學測量系統HZ_3〇〇〇(北斗 電工株式會社製),參考電極係使用銀/氯化銀電極 Ug/AgCl)。研磨墊係使用表面設有格子狀的溝槽之發泡聚 320663 28 200936309 胺酯墊(具有Χ-Υ凹槽之IC1000單層墊,ΝΙΤΤΑ HAAS株式 會社製)。 使用此裝置進行陽極分極測量(使基板的電極電位徐 徐增加),測量施加電壓與在基板流通的電流之關係。 第7圖係顯示導電膜的電位與電流密度的關係之曲線 圖。第7圖中,縱軸為電流密度,此電流密度表示在基板 上每單位的被研磨面積流通的電流。電流密度與研磨速度 具有電流密度愈大,則溶解到電解液之導電膜的溶解量變 ❹多,研磨速度就越快之關係。另外,第7圖中橫軸雖表示 電極電位,但因為在實際的研磨裝置中要以電極電位進行 控制會报麻煩,故一般係以被研磨基板與陰極之間的施加 電壓進行控制,所以在以下的說明中,關於基板的電極電 $控制’係採用施加電壓之表現。此外,施加電壓係表示 「作為陽極之基板的電極電位與作為陰極之支持構件(研 磨〇 )的電極電位之包含電解液的電位降低在内之陽極與 • 陰極的電位差」。 、 使pH 4至10之電解液與導電膜接觸然後使施加電壓 “加時,電流密度在預定的電麗會急遽地變化。使對於導 電膜的施加電壓從〇開始增加,電流密度會與電壓成比例 而增加,不過當電壓超過第一變化點(例如A點)之第一變 化電壓而繼續使電壓增加時,電流密度會從增加轉而減 少。繼而當電壓超過第二變化點(例如8點)之第二變化電 壓而繼續使電壓增加時,電流密度的減少程度會降低,然 後電流密度不再減少而成為大致一定值。此種現象可想成 320663 29 200936309 • 係因為在施加第一變化電壓以下的電壓時,導電膜的表面 形成有對於電解液而言為溶解性的保護膜,而在施加第二 變化電壓以上的電壓時,導電膜的表面會形成對於電解液 而言為不溶性的保護膜之緣故。 本案之發明人發現上述的第一變化電壓及第二變化電 壓會隨著基板W與研磨墊的接觸面壓而變化。第7圖中, 粗實線係接觸面壓為0.5 psi(接觸面壓為有限值,相當於 在導電膜表面之段差的上段部之硏磨)之情況,粗虛線係接 ❿觸面壓為0 psi(接觸面壓為0,相當於對導電膜表面之段 差的下段部)之情況。令接觸面壓為有限值時之第一變化點 為A點,接觸面壓為有限值時之第二變化點為B點,接觸 面壓為0時之第一變化點為C點,接觸面壓為0時之第二 變化點為D點(臨限值電壓)。接觸面壓愈高,第一及第二 變化電塵愈大,電流密度也愈大。使接觸面壓為0時之第 一變化電壓(C點電壓)及第二變化電壓(D點電壓),係分別 比使接觸面壓為有限值時之第一變化電壓(A點電壓)及第 二變化電壓(B點電壓)低0.5 V左右。 在此,令施加電壓在0至C點電壓之範圍為(2區域, 在C點電壓至B點電壓之範圍為β區域,在B點電壓以上 之範圍為7區域。另外,令施加電壓在C點電壓至Α點電 壓之範圍為5區域。 第8A至8C圖係對導電膜施加上述各區域之電壓時之 保護膜形成狀態之說明圖,第8A圖係α區域之情形、第 8Β圖係冷區域之情形、第8C圖係7區域之情形。 30 320663 200936309 施加α區域之電壓時,如第8A圖所 =二,容解性的保護媒71。在導電電 差之情況,在研磨塾101與導電膜66之 表面有& 之上段部Η,此保護膜71會被研磨而完全=為有限值 施加r區域之電壓時,如第8C圖所示, 解液50而言為不溶性的保護膜?2。在導會形成對於電 ❹Two money units are disposed on the opposite side of the traveling mechanism of the transport robot 202. The respective units 212 are disposed at positions reachable by the robot of the transport robot 202. Further, between the two drying units 212, a substrate station having four substrate mounting tables is disposed at a position where the transfer robot 2 () 2 can reach. A transfer robot 208 is disposed at a position where each of the drying unit 212 and the substrate station 206 can be reached. A washing unit 214 adjacent to the drying unit 212 is disposed at a position reachable by the robot arm of the transfer robot 208. The rotary conveyor 210' is disposed at a position where the robot arm of the transport robot 2G8 is reachable, and two electrolytic composite polishing apparatuses 25A of the present embodiment are disposed at a position where the substrate can be conveyed and received with the rotary conveyor 21. Each of the electrolytic composite polishing apparatuses 250 includes a substrate head 1, a polishing table 1A, a polishing pad 101 (see FIG. 2, etc.), and an electrolyte supply nozzle (electrolyte supply unit) that supplies an electrolytic solution to the polishing pad 1〇1. A dresser 218 for dressing the polishing pad 101 and a water tank 222 for cleaning the dresser 218. 16 320663 200936309 (Electrolysis composite grinding device) 2Fig. 2 Dry 2 Grinding ^ 250 schematic diagram. If the first = Λ: 1 is connected to the substrate head through the universal joint portion 1 = = the base f-head drive shaft 11 is coupled to the substrate head gas red m, : = 2 U1 is fixed to the swing arm 110. The substrate head driving shaft η is moved by the substrate head with the milk red 111, and the C2 spleen 151 is moved downward to lift the substrate head 1 as a whole, and the buckle which is fixed to the lower end of the substrate head body 2 (shirt ^咖) Ο 3 Press to the polishing table. The substrate gas ray is connected to the compressed air source 12 through the regulator, and the fluid pressure of the pressurized air supplied to the substrate head cylinder 1U can be adjusted by the regulator rei. The ring 3 presses the pressing force of the polishing pad ιοί. The substrate head drive shaft 11 is coupled to the rotating cylinder 112 via a key (not shown). The outer circumference of the rotating cylinder 112 is provided with a timing pulley 113. The swing head arm 110 is fixed with a base head motor 114 as a rotation drive unit, and the timing pulley 113 is connected to the timing pulley jig provided in the base head motor 114 through the timing belt 115. Therefore, the base head motor 114 is driven. Rotating, under the transmission of the timing pulley 116, the timing belt 115 and the timing pulley 113, the rotating cylinder 112 and the substrate head driving shaft 11 are integrally rotated to rotate the substrate head 1. The swing arm 110 is fixed and supported by The frame shaft 117 is supported, (substrate head). Fig. 3 is a cross-sectional view showing the substrate head 1. Fig. 4 is a bottom view of the substrate head 1 shown in Fig. 3. As shown in Fig. 3, the substrate head is shown. 1 has: internal containment space A cylindrical container-shaped substrate head body 2 and a solid 17 320663 200936309 - a buckle 3 fixed to the lower end of the substrate head body 2. The substrate head body 2 is made of a material having high strength and rigidity such as metal or ceramic. The buckle 3 is formed of a highly rigid resin such as PPS (polyphenylene sulfide) or an insulating material such as ceramic. The substrate head body 2 is provided with a cylindrical container-shaped case portion 2a and embedded. An annular pressure piece support portion 2b that is fitted to the inner side of the cylindrical portion of the case portion 2a, and an annular seal portion 2c that is interposed on the outer peripheral edge portion of the upper surface of the case portion 2a. The lower jaw portion of the buckle 3 on the lower surface of the casing portion 2a of the main body 2 protrudes inward. Further, the buckle 3 and the substrate head body 2 may be integrally formed with the center portion of the casing portion 2a of the substrate head body 2. The substrate head drive shaft 11 is provided, and the substrate head main body 2 and the substrate head drive shaft u are coupled by a universal joint portion 10. The universal joint portion 1 is provided with a substrate head body 2 and a substrate head drive shaft u. Spherical bearing mechanism capable of tilting motion with each other, and a woman who will be a substrate __ U Transferring to the rotation transmitting mechanism of the substrate head body 2 to transmit the pressing force and the rotational force of the substrate head driving shaft to the substrate head body while allowing the substrate head reading 2 to move obliquely with respect to the four members of the substrate head driving shaft 2. The spherical surface bearing mechanism is formed by a spherical recessed portion 11a formed on the lower surface of the substrate head drive shaft 11, and formed in the center of the upper surface of the housing portion 3, the moxibustion portion 2d, and the two concave portions Ua. Between 2d and formed by the bearing ball 12 formed by the ceramic material, the rotation transmission name is driven by the driving pin (not shown) fixed to the substrate head drive shaft 11 and the driven body part%. Not numb). Because even if the base (4) 320663 18 200936309 • the body 2 is tilted, the driven pin and the drive pin can move relative to each other in the up and down direction, so that the contact points between the two recesses and the bearing ball are offset, but the 'rotation transmitting mechanism can be surely The torque of the substrate head drive shaft n is transmitted to the substrate head body 2. The substrate head body 2 and the space formed by the inside of the buckle 3 integrally fixed to the substrate head body 2 are housed in an elastic pad 4 and a ring that abuts on the substrate W such as a semiconductor wafer held by the substrate head. The retaining ring 5 and the approximately disc-shaped refreshing plate supporting the elastic crucible 4 (the curry mountain (6) β 6. The outer peripheral portion of the elastic crucible 4 is clamped to the retaining ring 5 and fixed to the lower end of the retaining ring 5 Between the clamping plates 6, the lower surface of the clamping plate 6 is covered. Thereby, a space is formed between the elastic pad 4 and the clamping plate 6. The elastic between the retaining ring 5 and the substrate head body 2 is elastic. a pressure piece 7 formed of a film. The pressure piece 7 is made of, for example, Ethylene-Propylene Diene Monomer rubber (EPDM), p〇lyUrethane rubber, 矽Rubber (siUc〇nrubber), etc. The rubber sheet is formed of a rubber material having good strength and durability. The pressure piece 7 has one end sandwiched between the casing portion 2a of the substrate head body 2 and the pressure piece supporting portion 2b, and the other end of which is sandwiched at the upper end of the retaining ring 5. The portion 5a is fixed between the portion 5a and the stopper portion 5b. By the substrate head body 2, the clamping plate 6, and the protection The ring 5 and the pressure piece ' form a pressure chamber 21 inside the substrate head body 2. As shown in Fig. 2, a flow path 31 composed of a tube, a joint, or the like is extended from the pressure chamber 21, and the pressure chamber 21 is provided. The regulator RE2 in the flow path 31 is connected to the compressed air source 120. Further, the pressing piece 7 shown in Fig. 3 is formed of an elastic body such as rubber, 19 320663 200936309, and the pressing piece 7 is sandwiched. When the buckle 3 and the substrate head body 2 are fixed between each other, the lower surface of the buckle 3 may not have a desired plane due to the elastic deformation of the pressing piece 7 which is itself an elastic body. Therefore, in order to prevent this. In the present embodiment, the pressing piece supporting portion 2b is separately provided, and the pressing piece 7 is sandwiched between the case portion 2a of the substrate head main body 2 and the pressing piece supporting portion 2b, and is fixed to the elastic pad. 4, a center bag (center portion abutting member) 8 as an abutting member abutting against the elastic pad 4, and an annular pipe (outer abutting member) 9 are provided inside the space between the holding plate 6. In this example, as shown in FIGS. 3 and 4, the center bag 8 is disposed under the holding plate 6. The central portion, the annular tube 9 is disposed on the outer side of the central bag 8 so as to surround the central bag 8. Further, the elastic pad 4, the central bag 8 and the annular tube 9 are similar to the pressure piece 7 by, for example, three-way B. A rubber material having good strength and durability such as propylene rubber (EPDM), polyurethane rubber or ruthenium rubber is formed. As shown in Fig. 3, the space e formed between the holding plate 6 and the elastic pad 4 is in the center. A plurality of spaces are formed under the partition of the bag 8 and the annular tube 9, a pressure chamber 22 is formed between the central bag 8 and the annular tube 9, and a pressure chamber 23 is formed outside the annular tube 9. The central bag 8 is connected with the elastic pad 4 The elastic film 81, which abuts on the upper surface, is configured to detachably hold the central bag holder (holding cymbal) 82 of the elastic film 81. The central bag holder 82 is formed with a screw hole, and the screw 55 is locked to the screw hole to mount the center bag 8 = to the lower surface of the tablet 6. The middle portion of the pressure film 81 and the central bag holder 82 are formed with a central portion pressure chamber ice 20 320663 200936309 Similarly, the annular tube 9 is a strong film 9 that abuts against the upper surface of the elastic pad 4. And a ring member (holding portion) for holding the elastic film 91 in a detachable manner. (4) The configuration pipe holder 92 is formed with a screw hole 92a. [The screw 56 is locked to the screw hole (4), and the ring pipe can be mounted. The lower surface of the holding plate 6 is attached in a disassembled manner. The annular tube 9 is formed with an intermediate portion pressure 25 25 by means of the elastic film 91 and the annular tube holder 92, 23, a central pressure chamber 24, and a pressure chamber at the intermediate portion, respectively, and a pipe and a joint. The flow path of the configuration is connected from %%,%, and the pressure chambers 22 to 25 are connected to the compressed air source 12〇 as a supply source through the regulators (4), Cong, RE5, and halls provided in the respective flow paths 33 to %. . Further, the flow paths 31, 33 to 36 are connected to the respective regulators RE2 to RE6 through a rotary joint (not shown) provided at the upper end portion of the substrate head drive shaft 11#. Then, the pressurized fluid or the like pressurized air or the like is supplied to the pressure chamber 21 and the pressure chambers 22 to 25 above the holding plate 6 via the winding paths 31, 33 to 36 which communicate with the respective sound chambers. As shown in Fig. 2, the pressure of the pressurized fluid supplied to each of the pressure chambers can be adjusted by arranging the regulators RE2 to the legs on the flow paths 31, 33 to 36 of the pressures of 21 to 25. Thereby, the pressure inside the respective pressure chambers 21 to 25 can be independently controlled, or the pressure to the inside of 21 to 25 can be atmospheric pressure or vacuum. Thus, the pressures inside the pressure chambers 21 to 25 can be independently changed by the regulators RE2 to RE6, and the substrate ψ can be pressed to the polishing pad by the elastic pads for each of the substrates w (divided regions). I press 320663 200936309. As shown in Fig. 3, a plurality of convex portions 42 are erected from the holding plate 6 toward the pressure chambers 22, 23. The front end of the convex portion 42 is exposed to the elastic pad 4 through the opening portion 41. In addition, a flow path 43 extending from the front end surface of the convex portion 42 is provided, and the flow path 43 is connected to the vacuum source 121 shown in Fig. 2. Thus, the convex portion shown in Fig. 3 can be used. The front end surface of 42 absorbs the substrate W by vacuum suction. As shown in Fig. 2, the polishing table 1 of the electrolytic composite polishing apparatus 250 is embedded with a film thickness such as a eddy current of a conductive film or the like on the surface of the substrate. The sensor coil 228 of the ITM 226 formed by the sensor. The signal output by the ITM 226 is input to the control unit 310, and the output of the control unit 310 is used to control the regulators RE3 to RE6. (polishing table, grinding 塾) Fig. 5A is a schematic view showing the importance of the electrolytic composite polishing apparatus. A longitudinal section of the polishing table 100. A disk-shaped support member 254 254 is fixed to the upper surface of the polishing table 100. The support member 254 is made of a conductive material (metal, alloy, conductive plastic, etc.). There is a polishing pad 101, and the upper surface of the polishing pad 101 serves as a polishing surface. The polishing table 1 is coupled to a rotating mechanism (not shown), whereby the polishing table 100 can be rotated integrally with the support member 254 and the polishing pad 101. The supply nozzle 102 extends in the radial direction of the polishing pad 1〇 1. The electrolyte supply nozzle 102 is provided with a supply port 10a of the electrolyte solution. The supply port 102a is located above the central portion of the polishing pad ιοί An electrolyte supply source (not shown) is supplied to the center portion of the polishing crucible 1G1 through the electrolyte supply nozzle 1 2 and 22 320663 200936309. When the polishing pad 1G1 rotates, the electrolyte is wetted outward and filled. The substrate head 1 and the polishing pad 101 are interposed between the plurality of through holes lG1 of the polishing crucible 1Q1. The supporting member 254 is connected to the negative electrode of the power source 252 and has a function of a first electrode (drag pole). The wiring and the supporting member (the electrical contact of the cathode 254 is a roller, a brush, etc. For example, if the 筮q A solid β- Α 所 所, the electrical contact 262 can be The support member 254 and the i-face are in contact with each other. The electrical contact 262 is preferably formed of a soft metal core having a smaller specific resistance such as gold, silver, mesh, platinum, etc. The side of the polishing pad 101 is disposed with a power source. The positive electrode connection 252 of 252 is adhered to an a-pole (° electric electrode or application point) 264. The substrate head 1 is such that the substrate W and the blade are exposed to the side of the polishing crucible 101 to bring the substrate W into contact with the grinding surface. The lower surface will be in contact with the second electrode 264. Power is supplied from the /electrode 264 to the substrate. In addition, power is supplied from the second electrode 264 to the substrate. Conductive film. Thus, the supporting member 254 is connected to the conductive film on the substrate w as an anode. °, the electrolyte in the through hole 101a of the honing 101 and the electrical connection I 5 5B diagram schematically shows the other weight 254 of the electrolytic composite polishing apparatus. It is too ΓΓ ΓΓ 底 底 复合 复合 复合 复合 复合 复合 复合 复合 复合A coffee cup and a cover member 254a covering the upper surface of the bottom member. As described above, as the cathode (the first lightning striker structure 4) has at least j, the cover member 254a and the bottom member 254b are formed of a conductive material. 320663 23 200936309 Support member 254 cover shame and grinding A plurality of communication holes 255 are formed at the same position of the through hole 101a of the 塾ι〇. Further, a plurality of communication grooves 256 that are in communication with the communication holes are formed on the lower surface of the cover member 254a. A communication groove is provided on the upper surface of the base member 254b. The center portion of the polishing crucible 101 is formed with a first electrolyte solution receiving port 258A1 penetrating vertically through the polishing pad 1 (1), and is connected to the first electrolyte solution at the lid member 254a. The second electrolyte receiving port 25 is formed at the same position of the port 258A. The second electrolyte receiving port 258B communicates with the plurality of communication grooves 256. By the configuration of the supply port from the electrolyte supply nozzle 1〇2 The electrolyte supplied from 102a flows through the first electrolyte receiving port 258A, the second electrolyte receiving port 258B, the communication groove 256, and the communication hole 255 to reach the through hole 101a. Then, in the through hole 1〇la Internal formation The electrolytic solution of the grinding surface flows upward to supply the electrolytic solution to the polishing surface. (First embodiment, electrolytic composite polishing method)._ Next, the electrolytic composite polishing method according to the first embodiment will be described. Description of the substrate before polishing. The film structure of the substrate W to be polished according to the present embodiment will be described. A so-called low dielectric value (Low) is formed on the surface of the substrate W formed of tantalum or the like. -k) an interlayer insulating film 62 made of an insulating material such as siCh, SiOF, SiOC, etc. The surface of the interlayer insulating film 62 is formed with a contact plug or a recess 63 for forming a wiring. The surface of the interlayer insulating film 62 is formed with a barrier film 64 made of titanium, coarse, tungsten, tantalum, and/or an alloy of such a metal having a thickness of about nm. The barrier film 64 320663 200936309 1 The metal material of the conductive film 66 to be described later is prevented from diffusing to the substrate W, or is provided to improve the adhesion between the conductive film 66 and the interlayer insulating film 62. The surface of the barrier film 64 is formed of tungsten having a thickness of about 500 to 600 nm. Place When the conductive film 66 is formed by electrolytic plating, a seed film (not shown) as an electrode for electrolytic plating is formed on the surface of the barrier film 64. The surface of the conductive film 66 is formed. A recess 67 having a height of about 300 nm and a width of about 100 /zm is formed in the same manner as the recess 63 of the interlayer insulating film 62. Alternatively, it may be made of aluminum, copper, silver, gold or an alloy of such metals other than tungsten. The conductive film 66 is formed of a metal material. Since only the conductive film 66 filled in the recess 63 of the interlayer insulating film 62 is used as a contact plug or a metal wiring, the conductive film 66 formed on the outer side of the recess 63 is not required. Therefore, the excess conductive film 66 is removed by electrolytic composite polishing. Fig. 6B is an explanatory view of electrolytic composite polishing. In the electrolytic composite polishing system, the electrolyte solution 50 is brought into contact with the conductive film on the surface of the substrate W, and a voltage is applied to the conductive film 66, and the surface of the substrate W is pressed against the polishing pad 101 while the substrate W and the polishing pad 101 are moved (rotated). The surface of the conductive film 66 is ground. Since a plurality of wirings are laminated via the interlayer insulating film, it is necessary to flatten the surface of the substrate W in a state where the excess conductive film 66 is removed. The electrolytic composite polishing is to form a protective film 70 formed of an electrically insulating substance on the surface of the conductive film 66 by applying a voltage to the conductive film 66. The protective film formed on the upper portion of the conductive film 66 (outside of the concave portion 67) is removed by the polishing pad 101. Therefore, the upper portion of the guide 25 320663 200936309 electric film 66 will dissolve in the electrolyte 50 and be removed. On the other hand, the conductive film of the lower portion L (inside of the concave portion 67) is shielded by the protective film 7〇 and is not dissolved in the electrolytic solution 50. By the above electrolytic composite grinding, the step of the conductive film is eliminated. Thereby, as shown in Fig. 6C, the surface of the conductive film 66 and the surface of the exposed barrier film 64 are placed on the same plane, and the substrate W is planarized. However, the tungsten polishing method by CMP has a grinding rate that is low because the acid slurry using pH < 4 is used to form a relatively thick tungsten oxide film, and then the mechanical mechanism of grinding is performed mechanically. Therefore, the electrolytic composite polishing method of the present embodiment employs an electrolytic solution of ρ Η 4 to 10 to form a different protection from the conventional tungsten oxide film. Here, an electrolyte having a pH in the range of 4 to 1 Torr is used at the beginning of the processing. However, due to the hydrogen generated during processing, the pH of the electrolyte may change after the start of processing. Therefore, the pH of the electrolyte is in the range of 4 to 10, at least before processing starts, processing. The pH at the end of the process or at the end of the processing will fall within the range of 4 to 10, and the pH will fall within this range at the time of substantial processing. The measurement of Qiu value was carried out using a pH measuring device D51S (handheld) manufactured by H〇RIBA, with temperature correction and a glass electrode method (JIS Form 1). The measurement was carried out at room temperature between 2 ° C and 30 ° C. Further, in the present embodiment, substantially any electrolytic solution can be used as long as it has an appropriate electrical conductivity (about lmS/cm). The main electrolyte contained in the electrolytic solution is not limited as long as it can provide an appropriate conductivity and does not cause the surface of the conductive film to become thick. Further, it is preferred to form a complex with tungsten or a chelate of 26 320663 200936309 and it is preferred to include, for example, an organic acid. The organic acid is composed of a salt of glycolic acid, pyrophyllin, phytic acid, citric acid, vermiculic acid, maleic acid, malonic acid, lactic acid, tartaric acid, calcined acid, and the like. It is preferred that any one or a plurality of the selected ones in the group be a pH of the complex pH or a chelate of the compound which is easy to form a scale. The electrolyte may also contain a pH simple component. p (4) can use alkali metal salts, alkaline earth metal salts, etc., but in order to prevent metal contamination, ammonium salts are preferred. The electrolyte may also contain an additive that generates an electrically insulating substance. Additives that generate electrical insulating materials can utilize primary amine polymers, such as allylamine polymers (polymers with side chains only having primary amine groups, molecular weights of 1,000 to 60,000), allylamine hydrochloride polymers (molecular weight of 1,000 to 60' 000), allylamine hydrochloride, salt-diallylamine hydrochloride copolymer (molecular weight · 20,000 to 1 〇〇, 〇〇〇), allylamine sulfamate polymer (molecular weight ❹I2, 000), alkene Propylamine-diallylamine acetate copolymer (molecular weight 100,000), allylamine-dimethylallylamine copolymer (molecular weight 丨, 〇〇〇), 邛 is methylcarbonylated allylamine polymer (molecular weight 15,000) ), a partially methylcarbonylated allylamine acetate polymer (molecular weight: 15,000), and the like. Further, the primary amine polymer may also be polyethyleneimine (molecular weight L _ to 70, _). The polyethylenimine-based molecule has an I-form of a branched k which contains a -, a secondary, a tertiary amine, and has an effect because it has a -amine in the molecule. The preferred concentration of the additive which will generate the electrically insulating substance is from 0.01 to 5% by weight in the case of polyethyleneimine, more preferably from 〇 to 1% by weight, 27 320663 200936309, and the concentration is less than 0.01% by weight. The current suppression effect (electrical insulation) is low. On the other hand, when the concentration is higher than 5% by weight, the increase in the current suppression effect with respect to the increase in the amount of addition tends to decrease, so that the concentration is not high. More than 5 wt% is necessary. By adding such an additive which generates an electrically insulating substance, the voltage range in which the step elimination is high can be shifted to a low position as will be described later. In the case of CMP, the concentration of the abrasive grains must be 1% or more. However, in the present embodiment, the concentration is preferably 1% or less. Although this surfactant can also be added to improve the dispersibility of the abrasive particles, since the concentration of the abrasive grains is originally low, there is no problem even if it is not added. An example of the above electrolyte solution is ammonium citrate (pH 8) used in the present embodiment. "The polishing rate of tungsten" was invented by the inventors of the present invention by the method described below. 加工 The processing experiment was carried out using an electrolytic polishing apparatus capable of processing only a portion of the substrate equivalent to a diameter of 40 mm. The electrode potential of the metal film formed on the substrate is processed by applying a voltage while rubbing the exposed metal film with a polishing pad adhered to the rotating polishing table. For example, the current rate of 1 mA/cm 2 can be obtained at a polishing rate of 50 to 150 nm/min. The electrode potential is measured using an electrochemical measurement system HZ_3 (manufactured by Hokuto Denko Co., Ltd.). The reference electrode system uses a silver/silver chloride electrode Ug/AgCl. The polishing pad is made of a foamed poly 320663 28 200936309 surface with a lattice-like groove on the surface (an IC1000 single-layer pad with a Χ-Υ groove, ΝΙΤΤΑ HAAS Co., Ltd.) Using this device, the anode polarization measurement was performed (the electrode potential of the substrate was gradually increased), and the relationship between the applied voltage and the current flowing through the substrate was measured. Fig. 7 is a graph showing the relationship between the potential of the conductive film and the current density. In Fig. 7, the vertical axis represents the current density, which indicates the current flowing per unit of the polished area on the substrate. Current density and grinding The higher the current density is, the more the amount of dissolution of the conductive film dissolved in the electrolyte becomes larger, and the faster the polishing rate. In addition, although the horizontal axis in Fig. 7 indicates the electrode potential, it is in the actual polishing apparatus. Controlling the electrode potential is troublesome, and therefore it is generally controlled by the applied voltage between the substrate to be polished and the cathode. Therefore, in the following description, the electrode power control of the substrate is expressed by the applied voltage. The applied voltage indicates the potential difference between the anode potential and the cathode including the electrode potential of the substrate as the anode and the electrode potential of the supporting member (grinding crucible) serving as the cathode. The electrolyte of pH 4 to 10 is brought into contact with the conductive film and then the applied voltage is "added, the current density changes rapidly at a predetermined electric charge. The applied voltage to the conductive film is increased from the enthalpy, and the current density is related to the voltage. Increasingly, but when the voltage exceeds the first change voltage of the first change point (such as point A) and continues to increase the voltage, the current density will decrease from increasing to increasing. Then when the voltage exceeds the second change point (for example, 8 When the second change voltage of the point) continues to increase the voltage, the degree of reduction of the current density is reduced, and then the current density is no longer reduced to become a substantially constant value. This phenomenon can be thought of as 320663 29 200936309 • Because the first application is applied When the voltage is lower than the voltage, a surface of the conductive film is formed with a protective film which is soluble for the electrolytic solution, and when a voltage equal to or higher than the second varying voltage is applied, the surface of the conductive film is insoluble to the electrolytic solution. The inventor of the present invention found that the first varying voltage and the second varying voltage described above will follow the substrate W and the polishing pad. The contact surface pressure changes. In Fig. 7, the thick line contact surface pressure is 0.5 psi (the contact surface pressure is a finite value, which corresponds to the honing of the upper portion of the step on the surface of the conductive film), and the thick broken line is The contact pressure is 0 psi (the contact pressure is 0, which is equivalent to the lower section of the surface of the conductive film). The first change point when the contact surface pressure is a finite value is point A, contact surface pressure When the finite value is the second change point is B point, the first change point when the contact surface pressure is 0 is C point, and the second change point when the contact surface pressure is 0 is D point (the threshold voltage). The higher the surface pressure, the larger the first and second changes in electric dust, and the higher the current density. The first change voltage (point C voltage) and the second change voltage (point D voltage) when the contact surface pressure is zero, The first change voltage (point A voltage) and the second change voltage (point B voltage) are lower than about 0.5 V when the contact surface pressure is a finite value. Here, the applied voltage is in the range of 0 to C point voltage. For (2 areas, the voltage from point C to point B is in the range of β, and the range above the voltage at point B is 7 areas. The application voltage is in the range of the voltage from the point C to the voltage at the point C. The eighth embodiment is an explanatory diagram of the formation state of the protective film when the voltage of each of the regions is applied to the conductive film, and the eighth embodiment is the alpha region. In the case, the case of the 8th picture is the cold area, and the case of the 8C picture 7 area. 30 320663 200936309 When the voltage of the α area is applied, as shown in Fig. 8A = 2, the capacitive protective medium 71. In the case where the surface of the polishing crucible 101 and the conductive film 66 has an upper portion Η, the protective film 71 is ground and completely = when a voltage of the r region is applied for a finite value, as shown in FIG. 8C, the liquid is discharged. 50 is an insoluble protective film? 2. In the formation of the guide for electricity

差之情況,在研賴1αι與導電㈣之接⑽面^ 段部L,此保護膜72不會受到研磨而殘留下來/、、之下 相對於此,施加万區域之電麼時,會成為如 示之兩者中間的狀態。亦即,在研磨墊1〇1與“:= 接觸面壓為有限值之上段部1!會形成溶解性的保護膜,此 保護膜會被研磨去除掉。在研磨塾m與導電膜⑽之接 面壓為0之下段部L會形成不溶性的保護膜72,此 72·不會受到研磨而殘留下來。 5 、 本實施形態係將施加電壓維持在0區域而進行電解複 合研磨◊藉此,在上段部Η促進導電膜66溶解到電解液中, 在下段部L則抑制導電膜66溶解到電解液中。因此,可迅 速消除導電膜6 6的表面的段差。 另外,在施加/3區域之電壓的情況,因為覆蓋在保護 膜72下之下段部l的研磨速度相當缓慢,所以不易在導電 膜66發生碟形凹陷之情形。另外,因為可藉由調整施加壓 力來控制上段部Η的研磨速度,所以 < 將研磨塾1 〇 1與導 電膜66的接觸面壓設定得低些,而可抑制磨餘。例如,本 貫施形態可將以往進行CMP時之4 psi程度的接觸面壓, 320663 200936309 * 設定在2 Psi程度。此外,接觸面壓係為將基板頭按壓在 旋轉平台(也稱為台板(platen))之力除以與研磨塾接觸之 晶圓面積,亦即接觸面積之值所得到的值。此時,貫通研 磨墊之貫通孔所佔的區域要從該接觸面積減掉。 如上所述,電流密度與研磨速度具有電流密度愈大, 研磨速度就越快之關係。 如第7圖所示,在施加電壓為〇至c點電壓之〇:區域, 使接觸面壓為有限值(〇·5 psi)時以及使接觸面壓為〇(〇 ❿ psi)時’電流密度都會隨著電壓之增加而增加。相對於此, 在C點電壓至A點電壓之(5區域,使接觸面壓為有限值時 之電流密度雖會繼續增加,但使接觸面壓為〇時之電流密 度卻會轉而減少。因此,在<5區域之使接觸面壓為有限值 時與使接觸面壓為0時之電流密度的差,通常比在α 區域之電流密度的差△ I a大。使接觸面壓為有限值時與使 接觸面壓為0時之電流密度的差,實際上係對應於導電膜 表面之段差的上段部與下段部之研磨速度的差。因此,將 施加電壓維持在5區域而進行研磨,導電膜表面之段差的 上段部與下段部之研磨速度的差會變大,所以可迅速消除 導電膜表面的段差。 帛7 ®中’粗線表示電解衫含有會生成電氣絕緣性 物質之从、加;=!]的If况’細線表不添加了聚乙亞胺(观)1重 量%作為會生成電氣絕緣性物f之添加_情況。此外,實 線係研磨整與基板的接觸面壓為0.5 psi的情況,虛線係 接觸面壓為0 psi的情況。 320663 32 200936309 * 已知在不含有會生成電氣絕緣性物質之添加劑(或濃 度很低)的情況’電流密度會變高。其理由可想成是因為會 生成電氣絕緣性物質之添加劑的濃度愈高愈會形成強固的 保護膜,而難以藉研磨將保護膜去除掉之緣故。因此’希 望提高研磨速度時’只要使用會生成電氣絕緣性物質之添 加劑的濃度低之電解液即可。反之,為了進行薄導電膜的 研磨或進行正確的研磨停止而希望降低研磨速度時,可使 用會生成電氣絕緣性物質之添加劑的濃度高之電解液。此 ❺外從第7圖可知:在不含有會生成電氣絕緣性物質之添加 劑(或濃度很低)的情況,第一及第二變化電壓會變高。因 此,最好依據會生成電氣絕緣性物質之添加劑的激度來調 整施加電壓。 第9圖係顯示使電解液的pH變化時之施加電壓與電流 密度的關係之曲線圖。第9圖的實驗採用pH 4, pH 6, pH 8, pH 9之電解液(沒有會生成電氣絕緣性物質之添加劑)。 ❾ 已知電解液的PH愈大,電流密度會變高。其理由可神 成是因為電解液的PH愈大愈會促進導電膜的溶解之緣 故。因此,希望提高研磨速度時,可使用pH大之電解液。 反之,希望降低研磨速度時’可使用pH小之電解液。此外 從第9圖可知:電解液的pH愈大,第一及第二變化電壓會 變高。因此,最好依據電解液的PH來調整施加電壓。 第10圖係顯示使研磨墊的轉速變化時之施.加電壓與 電流密度的關係之曲線圖。第圖的實驗採用不含有會生 成電氣絕緣性物質的添加劑之電解液。第10圖中,粗線係 320663 33 200936309 ’ 轉速為250 rpm的情況,細線係轉速為50 rpm的情況。此 外’實線係研磨墊與基板的接觸面壓為〇.5 psi的情況, 虛線係接觸面壓為〇 psi的情況。 已知研磨墊的轉速愈大,電流密度會變高。其理由可 想成是因為研磨墊的轉速愈大,保護膜的去除進行得愈 快,而促進導電膜的溶解之緣故。因此,希望提高研磨速 度時’可提高研磨墊的轉速。反之,希望降低研磨速度時, 可降低研磨墊的轉速。研磨墊的轉速也可在研磨進行中加 ❿ 以變化。此外從第1〇圖可知:研磨墊的轉速愈大,第一及 第二變化電壓會變高。因此,最好依據研磨墊的轉速來調 整施加電壓。 (第二實施形態、電解複合研磨方法) 接著’針對第二實施形態之電解複合研磨方法進行說 明。 第一實施形態係將對於導電膜之施加電壓維持在預定 ❹範圍而進行研磨工序。相對於此,第二實施形態係在研磨 工序之前’進行對導電膜施加預定電壓而形成保護膜之保 護膜形成工序,此點與第一實施形態不同。以下,構成上 與第一實施形態一檬的部份之詳細說明,將予以省略。 首先’進行使電解液與基板表面的導電膜接觸並施加 電壓至導電膜,藉以在導電膜的表面形成保護膜之保護膜 形成工序。此處,係施加接觸面壓為〇時之第二變化點(例 如第7圖中之D點)之第二變化電壓以上的電壓。藉此,可 想像得到’會如第8C圖所示,形成對於電解液50而言為 34 320663 200936309 ’不溶性的保護膜72。此保護膜72形成於導電膜66的整個 表面且為不<逆的,即使將施加電壓降到第二變化電壓以 下也不會變化。 在此保護膜形成工序之後,進行通常之電解複合研磨 工序。如此〆來,形成於導電膜66的上段部U之保護膜 72雖會被研磨去除掉’但形成於導電膜66的下段部L之 保護膜72並不會受到研磨而殘留下來。藉此,在上段部η 促進導電膜66溶解到電解液中,在下段部l則抑制導電膜 © 66溶解到電解液中。因此,可迅速消除導電膜66的表面 的段差。 (變形例) 亦可在上述之保護膜形成工序之後,進行化學機械研 磨(CMP)工序。 第11圖係CMP裝置之概略圖<Μρ係一邊將研磨漿犯 供給至基板W表面的導電膜,一邊將基板w表面按壓至研 ❺磨塾101同時使基板W與研磨塾101相對移動,而研磨導 電膜的表面者。即使是在保護膜形成工序之後進行哪工 序之情況也-樣’如第8C圖所示之形成於導電膜66的上 段部Η之保護膜72雖會被研磨去除掉,但形成於導電膜 66的下段部L之保護臈72並不會受到研磨而殘留下來。 藉此,在上段部Η促進導電膜66溶解到電解液中,在下段 部L則抑制導電膜66溶解到電解液中。因此,可迅速消除 導電膜6 6的表面的段差。 此外,本發明之技術範圍,並非限定於上述的實施形 320663 35 200936309 献其變形例者’而是包含:在不脫離本發明宗旨的範圍 内除了上述的實施形態等之外還加上種種的變化者。亦 即,在實施形態等所舉的具體的材料及構成等只不過是一 個例子,仍然可做適當的變化。 (研磨墊) 另外,亦可採用以下的東西來作為研磨墊。 關於研磨塾的種類,舉例來說有獨立發泡聚胺酯墊及 連續發狀廣皮(suede)墊。料,在使用不含磨粒的電解 ©液之情況,可使用藉結合劑使磨粒相互黏結而作成的固定 磨粒墊。上述磨粒可採用:氧化鈽(Ce〇2)、氧化鋁(a12〇3)、 碳化矽(SiC)、氧化矽(Si〇2)、氧化锆(Zr〇2)、氧化鐵(Fe〇, Fe2〇3,Fe3〇4)、氧化錳(Mn〇2, Mm〇3)、氧化鎂(Mg〇)、氧化 #5(Ca0)、氧化鋇(BaO)、氧化鋅(Zn〇)、碳酸鋇(Bac〇3)、 碳酸鈣(CaC〇3)、鑽石(C)、或上述材料的複合材料。另外, 結合劑可採用:酚樹脂、胺基塑料樹脂(amin〇plast ⑩resin)、胺甲酸醋樹脂、環氧樹脂、丙烯酸樹脂、丙烯酸 化異三聚氰酸樹脂、尿素-曱醛樹脂、異三聚氰酸樹脂、丙 烯酸化胺曱酸酯樹脂、丙烯酸化環氧樹脂等。另外,為了 確保對於被研磨對象之導電膜表面之給電,亦可使用在研 磨表面之至少一部份具有導電面之導電性墊。 此處,關於研磨墊的溝槽形狀,可形成為一個以上的 (1)同心圓溝槽、(2)偏心溝槽、(3)多角形溝槽(包含格子 溝槽)、(4)螺旋溝槽、(5)放射溝槽、(6)平行溝槽、(7) 弧形溝槽、或此等溝槽的組合。此等溝槽形狀會影響電解 320663 36 200936309 μ## ’心si溝槽及偏心溝槽因為立流 路封閉所以具有將電解液保持在研磨墊上之效果。相對於 此,多角形溝槽及放射溝槽具有促進電解液流人到研磨對 象及排出到研磨墊外之m外’為了提高電解液流入 到基板的被加工表面内、從基板的被加工表面内流出及保 持在基板的被加工表面内之效率’亦可適當地調整研磨蟄 面内之溝槽寬度、溝槽節距、溝槽深度而調整研磨墊内的 溝槽密度分佈。 例如,溝槽寬度、溝槽深度可為〇,4mm以上,溝槽節 距為溝槽寬度的兩倍以上,若考量到電解液之流動,則溝 槽寬度、溝槽深度為〇. 6丽以上較佳。另外,為了活化溝 槽間之電解液㈣動,可在龍間設㈣㈣槽(例如形成 於同心圓溝槽間之複數個細溝槽、形成於粗格子溝槽間之 細溝槽.等)。此外,關於賴的斷面形狀,.可採用四角形溝 槽、圓形溝槽以及V形溝槽。另外,要促進電解液從溝槽 排出夺可考慮安裝著研磨墊之研磨台的旋轉方向,而形 f向旋轉方向下游傾斜之順向溝槽。反之,要抑制電解液 =溝槽排出時’可形成向旋轉方向上游側傾斜之逆向溝 才曰。再者,為了保持電解液,可在研磨墊表面形成一個以 上的貫通孔。 另外研磨墊與晶圓的接觸面形狀會影響將由於電解 ’、生成之保護皮膜去除之機械作用。為了增加接觸面 =產生的機_用,可使接觸面形狀為銳利的形狀,舉例 〜'有圓錐形、多角錐形、金字塔形、稜鏡形等。此處, 320663 37 200936309 •依被研磨物而定,若接觸面形狀過於銳利則會成為造成到 痕等的原因,避免這種情形的方法是將接觸面形狀形成為 例如圓錐台或角錐台之類之上面平坦化的形狀。另外,使 接觸面所產生的機械作用更加降低之形狀’舉例來說有圓 柱形、橢圓柱形、半球形等。這些形狀的配置可為格子、 鋸齒狀、三角配置之類的有規則性的形式,或是為了消除 規則性而配置成任意的形式。另外,這些形狀可在研磨墊 的研磨面内存在有複數種以上,亦可調整其密度分佈。 ❹(膜厚檢知感測器) 第2圖之實施形態中顯示的雖然是使用渦電流感測器 作為檢測導電臈的殘留膜厚之方法的例子,但除此之外亦 可利用光學式監測器、螢光X射線膜厚測量、電壓-電流的 變化檢測等。 -光學式監測器因為係利用反射光強度由於光干涉而變 化的現象而進行監測者,所以可利用從埋設於研磨台内之 光源通過研磨墊的孔而照射測量光之方法、或在使基板突 ® 懸於研磨台外之狀態進行測量之方法等。此外,因為變化 開始點會隨著所使用的光的波長不同而不同,所以波長要 針對被研磨材料而適當選擇。 螢光X射線膜厚測量因為係利用對測量對象照射一次 X射線之際產生之螢光X射線的強度會對應於膜厚而變化 之現象進行測量者’所以係在研磨中從埋設於研磨台内之 X射線源對導電膜照射一次X射線而進行測量。 電壓-電流的變化檢測係利用電阻會隨著測量對象之 320663 38 200936309 導電膜的膜厚而變化之現象進行檢測者。其係藉由使電壓 一定而測量電流的變化、或使電流一定而測量電壓的變 化,而從電阻算出膜厚之方法。依照此方法則只要監測研 磨令的電壓、電流就可進行膜厚的檢知,所以可簡便地利 用。 另卜在例如阻P早膜上之導電膜的研冑中或包含絕緣 膜上的阻障膜之導電膜的研磨中將導電膜之研磨已經 的狀態⑽磨終點)予以檢測出之方法,除了上述的膜^ 貝j方法之外’舉例來說還有:監測研磨塾表面溫度或基板 表面溫度的變化之方法、監測基板與研磨墊間的摩擦力的 變化之方法、監測表面影像的變化之方法、監測研磨裝或 電解液中的成分(副生成物的氧化物濃度、源自於導電膜的 離子濃度)的變化之方法等。 Y監測研磨墊表面溫度或基板表面溫度的變化之方法, 可採用:以放射溫度計量測研磨塾表面溫度、或以埋設於 ❹研磨台内之放射溫度計通過設於研磨墊的孔而量測基板表 面的溫度之方法。 監測基板與研磨墊間的摩擦力的變化之方法,可採 用.測里安裝有研磨墊之研磨台或基板保持件的驅動電流 的變化、或針對基板保持件測量特定頻率的振動振幅隨時 間的變化之方法。 監測基板表面影像的變化之方法,可採用:以埋設於 研磨台内之色度感測器通過設於研磨墊的孔而測量基板表 面的色調的變化、或測量利用CCD取得之基板表面的二維 39 320663 200936309 影像的變化之方法。 監測研磨漿或電解液中的成分(副生成物的氧化物濃 度、源自於導電膜的離子遭度)的變化之方法,可採用:量 測從研磨台排出的研磨液中之源自於導電膜的離子濃度的 變化之方法。 根據本發明,在導電臈的表面有段差之情況,會在導 電膜與研磨墊的接觸面壓為有限值之上段部形成溶解性的 保護膜,此保護膜會被研磨而完全去除掉。另外,在導電 ©膜與研磨墊的朗面㈣G之下段部軸不溶性的保護 膜,此保護膜不會被研磨而殘留下來。藉此,在上段部促 =導電膜溶解到電解液中,在下段部抑制導電膜之溶解。 因此,可迅速消除導電膜表面的段差。 ★接著’根據圖式說明本發明:第三實施形態。 (第二實施形態)(基板處理裝置) 、關於基板處理裝置的構成,因與前面的實施形態中說 ❹ I的相㈤所以將兩者共通部份的說明予以省略。 如同在刚面的實施形態中說明過的,在第2圖中,藉 由凋希器RE2至RE6使各壓力室21至25的内部的壓力可 獨立變化’就可針對基板w的各個部份(劃分區域)調整透 過彈性塾將基板w按壓至研磨塾繼之按壓力(作用到基板 表面之接觸面壓)。 換舌之,如第4圖所示,利用各壓力室21至25在研 磨中適虽调整扣環3按壓研磨塾101之按壓力、以及將基 板W按[至研磨墊iQi之按壓力,就可將基板▽的中心部 40 320663 200936309 , (第4圖之c】),以及從中心部到中間部(C2)、外圍部(C3)、 然後到周緣部(C4)、再到位於基板w的外側之扣環3的外 周部等各個部份的研磨壓力(作用到基板表面之接觸面壓) 之分佈設定為所希望的值。 如此,就可將基板W劃分為同心之四個圓及圓環部份 (C1至C4) ’且以獨立的按壓力按麼各個部份(按遷區域)。 研磨速度雖與對於基板#的被研磨面之按壓力有關係,但 因為可如上述般控制各部份的按壓力,所以可獨立控制基 ❹板W的四個部份(C1至C4)之研磨速度。因此,即使基板^ 的表面之要硏磨的膜在半徑方向的膜厚分佈不均勻,也能 夠使基板W的整個面都不發生研磨不足或過度研磨的情 形。 亦即,即使在基板w的表面之要研磨的膜其膜厚隨著 在基板W半徑方向的位置不同而不同之情況,也只要藉由 使上述各壓力室21至25之中位於基板¥的表面的膜厚較 ❹厚部份的上方之壓力㈣壓錢其他壓力錢壓力高、或 使位於基板W的表面的膜厚較薄部份的上方之壓力室的壓 力比其他壓力室的壓力低,可使對於膜厚較厚部份的被研 磨面的按壓力比對於膜厚較薄部份的被研磨面的按壓力 大,就可選擇性地提高該部份的研磨速度。藉此,不管成 膜時的膜厚分佈為何,都可在研磨基板W整個面進行不 過度且無不足的研磨。 另外,在本實施形態之研磨台中,位於研磨墊1〇1的 侧邊的位置配置有連接至電源252的正極之給電電極(施 320663 41 200936309 加點)264。基板頭1係以讓基板W的一部份在研磨墊101 的侧邊露出之狀態使基板W與研磨面接觸,使基板W的下 表面之周緣部C4會與給電電極264接觸。藉此,從給電電 極264施加至基板W的導電膜66。另外,亦可透過扣環而 從給電電極264施加至基板w的導電膜66。於是,作為陰 極之支持構件254與作為陽極之基板w上的導電膜通過充 填於研磨墊101的貫通孔l〇la中之電解液而電性連接。 (電解複合研磨方法)In the case of a difference, in the case where the 1α1 and the conductive (4) are connected to the (10) surface portion L, the protective film 72 is not left to be polished and/or underneath. The state between the two is shown. That is, in the polishing pad 1〇1 and the “:= contact surface pressure is a finite value above the segment 1!, a solubility protective film is formed, and the protective film is removed by grinding. In the polishing 塾m and the conductive film (10) When the junction pressure is 0, the in-situ portion L forms an insoluble protective film 72, and this 72· remains without being polished. 5. In this embodiment, the applied voltage is maintained in the 0 region, and electrolytic composite polishing is performed. In the upper portion, the conductive film 66 is promoted to dissolve in the electrolytic solution, and the lower portion L suppresses dissolution of the conductive film 66 into the electrolytic solution. Therefore, the step difference of the surface of the conductive film 66 can be quickly eliminated. In the case of the voltage, since the polishing speed of the lower portion 1 covered under the protective film 72 is relatively slow, it is difficult to cause dishing of the conductive film 66. In addition, since the pressure can be adjusted to control the upper portion Since the polishing rate is set, the contact surface pressure between the polishing 塾1 〇1 and the conductive film 66 is set lower, and the grinding residue can be suppressed. For example, the conventional embodiment can be used for the contact surface of 4 psi in the conventional CMP. Pressure, 320663 200 936309 * Set at 2 Psi. In addition, the contact surface pressure is the force that presses the substrate head against the rotating platform (also known as the platen) divided by the area of the wafer that is in contact with the polishing pad, ie the contact area. The value obtained by the value. At this time, the area occupied by the through hole penetrating the polishing pad is subtracted from the contact area. As described above, the current density and the polishing rate have a relationship that the current density is higher and the polishing rate is faster. As shown in Figure 7, the voltage is applied to the 〇: region of the voltage at point c, and the contact surface pressure is finite (〇·5 psi) and the contact surface pressure is 〇(〇❿ psi). The density will increase with the increase of the voltage. In contrast, the voltage at point C is increased to the voltage at point A (in the 5 region, the current density at the contact surface pressure is increased, but the contact surface pressure is increased. At this time, the current density will decrease. Therefore, the difference in current density when the contact surface pressure is finite in the <5 region and the contact surface pressure is 0 is usually smaller than the difference in current density in the α region. △ I a is large. When the contact surface pressure is finite, The difference in current density when the contact pressure is 0 is actually the difference in the polishing speed of the upper portion and the lower portion corresponding to the step difference of the surface of the conductive film. Therefore, the applied voltage is maintained in the region of 5, and the surface of the conductive film is polished. The difference between the polishing speeds of the upper and lower sections of the step becomes larger, so that the step of the surface of the conductive film can be quickly eliminated. The thick line in 帛7® indicates that the electrolytic shirt contains the slaves that generate electrical insulating substances; The condition of '] is not added to the fine line table by adding 1% by weight of polyethyleneimine (as shown) as the addition of electrical insulating material f. In addition, the contact pressure of the solid line to the substrate is 0.5 psi. In the case of a dotted line, the contact pressure is 0 psi. 320663 32 200936309 * It is known that the current density does not increase when the additive (or the concentration is very low) which generates an electrically insulating substance is not contained. The reason for this is conceivable because the higher the concentration of the additive which generates the electrically insulating substance, the stronger the protective film is formed, and it is difficult to remove the protective film by polishing. Therefore, when it is desired to increase the polishing rate, it is sufficient to use an electrolyte having a low concentration of an additive which generates an electrically insulating substance. On the other hand, in order to reduce the polishing rate in order to perform polishing of the thin conductive film or to stop the correct polishing, an electrolyte having a high concentration of an additive which generates an electrically insulating substance can be used. Further, it can be seen from Fig. 7 that the first and second varying voltages become high when the additive (or the concentration is low) which generates an electrically insulating substance is not contained. Therefore, it is preferable to adjust the applied voltage in accordance with the sensitivity of the additive which generates the electrically insulating substance. Fig. 9 is a graph showing the relationship between the applied voltage and the current density when the pH of the electrolytic solution is changed. The experiment in Figure 9 uses an electrolyte of pH 4, pH 6, pH 8, pH 9 (no additives that will generate electrical insulating materials). ❾ It is known that the higher the pH of the electrolyte, the higher the current density. The reason for this is because the higher the pH of the electrolyte, the more the dissolution of the conductive film is promoted. Therefore, when it is desired to increase the polishing rate, an electrolyte having a large pH can be used. Conversely, when it is desired to reduce the polishing rate, an electrolyte having a small pH can be used. Further, it can be seen from Fig. 9 that the higher the pH of the electrolyte, the higher the first and second varying voltages. Therefore, it is preferable to adjust the applied voltage depending on the pH of the electrolyte. Fig. 10 is a graph showing the relationship between the applied voltage and the current density when the rotational speed of the polishing pad is changed. The experiment in the figure uses an electrolyte that does not contain an additive that will generate an electrically insulating substance. In Fig. 10, the thick line is 320663 33 200936309 ' when the rotation speed is 250 rpm, and the thin line speed is 50 rpm. Further, the solid-line polishing pad has a contact surface pressure of 〇5 psi with the substrate, and the dotted line has a contact surface pressure of 〇 psi. It is known that the higher the rotational speed of the polishing pad, the higher the current density. The reason for this is considered to be that the higher the rotational speed of the polishing pad, the faster the removal of the protective film is, and the dissolution of the conductive film is promoted. Therefore, it is desirable to increase the rotational speed of the polishing pad when the polishing speed is increased. Conversely, when it is desired to reduce the polishing speed, the rotational speed of the polishing pad can be lowered. The rotational speed of the polishing pad can also be varied by changing during the grinding process. Further, it can be seen from the first diagram that the higher the rotational speed of the polishing pad, the higher the first and second varying voltages. Therefore, it is preferable to adjust the applied voltage in accordance with the rotational speed of the polishing pad. (Second embodiment, electrolytic composite polishing method) Next, the electrolytic composite polishing method according to the second embodiment will be described. In the first embodiment, the polishing process is performed while maintaining the applied voltage of the conductive film in a predetermined range. On the other hand, the second embodiment differs from the first embodiment in that a protective film forming step of applying a predetermined voltage to the conductive film to form a protective film is performed before the polishing step. Hereinafter, a detailed description of the configuration of the first embodiment and the first embodiment will be omitted. First, a protective film forming step of bringing an electrolytic solution into contact with a conductive film on the surface of the substrate and applying a voltage to the conductive film to form a protective film on the surface of the conductive film is performed. Here, a voltage equal to or higher than the second variation voltage of the second change point (e.g., point D in Fig. 7) when the contact surface pressure is 〇 is applied. Thereby, it is conceivable that a protective film 72 which is 34 320663 200936309 'insoluble to the electrolytic solution 50 is formed as shown in Fig. 8C. This protective film 72 is formed on the entire surface of the electroconductive film 66 and is not <inverse, and does not change even if the applied voltage is lowered to the second variation voltage. After this protective film forming step, a usual electrolytic composite polishing step is performed. As a result, the protective film 72 formed on the upper portion U of the conductive film 66 is polished and removed, but the protective film 72 formed on the lower portion L of the conductive film 66 is not left by polishing. Thereby, the upper portion η promotes dissolution of the conductive film 66 into the electrolytic solution, and in the lower portion 1 suppresses dissolution of the conductive film © 66 into the electrolytic solution. Therefore, the step difference of the surface of the conductive film 66 can be quickly eliminated. (Modification) A chemical mechanical polishing (CMP) step may be performed after the above-described protective film forming step. Fig. 11 is a schematic view of a CMP apparatus. Μ 系 系 系 系 系 系 系 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 一边 , 一边 , And the surface of the conductive film is polished. Even if the process is performed after the protective film forming step, the protective film 72 formed on the upper portion of the conductive film 66 as shown in FIG. 8C is polished and removed, but is formed on the conductive film 66. The protective layer 72 of the lower portion L is not left to be ground by grinding. Thereby, the conductive film 66 is promoted to dissolve in the electrolytic solution in the upper portion, and the conductive film 66 is prevented from being dissolved in the electrolytic solution in the lower portion L. Therefore, the step difference of the surface of the conductive film 66 can be quickly eliminated. In addition, the technical scope of the present invention is not limited to the above-described embodiment 320663 35 200936309, but includes various modifications in addition to the above-described embodiments and the like without departing from the scope of the present invention. Change. That is, the specific materials, configurations, and the like given in the embodiments and the like are merely examples, and appropriate changes can be made. (Polishing pad) In addition, the following things can also be used as a polishing pad. Regarding the type of the abrasive mash, there are, for example, a separate foamed polyurethane pad and a continuous hair suede pad. In the case of using electrolysis without abrasive particles, a fixed abrasive pad made by bonding the abrasive particles to each other by using a binder may be used. The above abrasive grains may be: cerium oxide (Ce〇2), aluminum oxide (a12〇3), cerium carbide (SiC), cerium oxide (Si〇2), zirconia (Zr〇2), iron oxide (Fe〇, Fe2〇3, Fe3〇4), manganese oxide (Mn〇2, Mm〇3), magnesium oxide (Mg〇), oxidation #5 (Ca0), barium oxide (BaO), zinc oxide (Zn〇), barium carbonate (Bac〇3), calcium carbonate (CaC〇3), diamond (C), or a composite of the above materials. In addition, the bonding agent can be: phenol resin, amine-based plastic resin (amin〇plast 10resin), urethane resin, epoxy resin, acrylic resin, acrylated isocyanuric resin, urea-furfural resin, different A polycyanate resin, an acrylated amine phthalate resin, an acrylated epoxy resin, or the like. Further, in order to secure the power supply to the surface of the conductive film to be polished, a conductive pad having a conductive surface on at least a part of the polishing surface may be used. Here, regarding the groove shape of the polishing pad, one or more (1) concentric circular grooves, (2) eccentric grooves, (3) polygonal grooves (including lattice grooves), and (4) spirals may be formed. a groove, (5) a radiation groove, (6) a parallel groove, (7) an arc groove, or a combination of such grooves. These groove shapes affect the electrolysis 320663 36 200936309 μ## 'the heart si groove and the eccentric groove have the effect of holding the electrolyte on the polishing pad because the vertical flow path is closed. On the other hand, the polygonal groove and the radiation groove have a function of promoting the flow of the electrolyte to the object to be polished and discharged to the outside of the polishing pad, in order to increase the flow of the electrolyte into the surface to be processed of the substrate, from the processed surface of the substrate. The efficiency of the inner flow and the retention in the machined surface of the substrate can also be adjusted by appropriately adjusting the groove width, the groove pitch, and the groove depth in the polishing face to adjust the groove density distribution in the polishing pad. For example, the groove width and the groove depth may be 〇, 4 mm or more, and the groove pitch is more than twice the groove width. If the flow of the electrolyte is considered, the groove width and the groove depth are 〇. The above is preferred. In addition, in order to activate the electrolyte (four) movement between the grooves, a (four) (four) groove may be provided between the dragons (for example, a plurality of fine grooves formed between the concentric grooves, a fine groove formed between the coarse lattice grooves, etc.) . Further, regarding the sectional shape of the Lay, a quadrangular groove, a circular groove, and a V-shaped groove may be employed. Further, in order to promote the discharge of the electrolyte from the groove, the direction of rotation of the polishing table to which the polishing pad is mounted may be considered, and the shape f may be inclined toward the downstream direction in the direction of rotation. On the other hand, in order to suppress the electrolyte = when the groove is discharged, the reverse groove which is inclined toward the upstream side in the rotational direction can be formed. Further, in order to maintain the electrolyte, one or more through holes may be formed in the surface of the polishing pad. In addition, the shape of the contact surface of the polishing pad with the wafer affects the mechanical action of removing the protective film formed by electrolysis. In order to increase the contact surface = the machine used, the shape of the contact surface can be sharp, for example, 'conical, polygonal, pyramidal, 稜鏡-shaped, etc. Here, 320663 37 200936309 • Depending on the object to be polished, if the shape of the contact surface is too sharp, it may cause a mark or the like. The method to avoid this is to form the shape of the contact surface into, for example, a truncated cone or a truncated cone. The shape that is flattened above the class. Further, the shape which makes the mechanical action generated by the contact surface more reduced' is exemplified by a cylindrical shape, an elliptical cylindrical shape, a hemispherical shape, and the like. The configuration of these shapes may be in the form of a regularity such as a lattice, a zigzag, a triangular configuration, or may be configured in any form in order to eliminate the regularity. Further, these shapes may be plural or more in the polishing surface of the polishing pad, and the density distribution thereof may be adjusted. ❹ (Thickness Detecting Sensor) Although the eddy current sensor is used as an example of a method of detecting the residual film thickness of the conductive raft as shown in the embodiment of Fig. 2, an optical type may be used. Monitor, fluorescent X-ray film thickness measurement, voltage-current change detection, etc. - The optical monitor is monitored by a phenomenon in which the intensity of the reflected light changes due to light interference, so that the method of irradiating the measurement light from the light source embedded in the polishing table through the hole of the polishing pad or the substrate can be used The method of measuring the state of the protrusion® outside the polishing table. Further, since the starting point of the change differs depending on the wavelength of the light used, the wavelength is appropriately selected for the material to be polished. The measurement of the thickness of the fluorescent X-ray film is performed by the phenomenon that the intensity of the fluorescent X-ray generated when the X-ray is irradiated once to the measurement target changes depending on the thickness of the film, so that it is buried in the polishing table during polishing. The X-ray source inside is measured by irradiating the conductive film with X-rays once. The voltage-current change detection method uses a phenomenon in which the resistance changes depending on the film thickness of the conductive film of the measurement object 320663 38 200936309. This is a method of calculating the film thickness from the electric resistance by measuring the change in the current by making the voltage constant or by measuring the change in the voltage while the current is constant. According to this method, the film thickness can be detected by monitoring the voltage and current of the grinding order, so that it can be easily used. Further, a method of detecting the state (10) of the polishing of the conductive film in the polishing of the conductive film on the resistive film or the polishing of the conductive film including the barrier film on the insulating film, in addition to the method of detecting the state in which the conductive film has been polished (10) In addition to the above-mentioned method, there are, for example, a method of monitoring the change in the surface temperature of the polishing crucible or the surface temperature of the substrate, a method of monitoring the change in the friction between the substrate and the polishing pad, and monitoring the change of the surface image. A method of monitoring a change in a component (a concentration of an oxide of a by-product, an ion concentration derived from a conductive film) in a polishing apparatus or an electrolytic solution, or the like. The method of monitoring the change of the surface temperature of the polishing pad or the surface temperature of the substrate may be: measuring the surface temperature of the polishing crucible by the radiation temperature, or measuring the substrate through the hole provided in the polishing pad by a radiation thermometer embedded in the crucible polishing table. The method of the temperature of the surface. The method of monitoring the change of the friction between the substrate and the polishing pad may be performed by using a variation of the driving current of the polishing table or the substrate holder on which the polishing pad is mounted, or measuring the vibration amplitude of the specific frequency with respect to the substrate holder over time. The method of change. The method for monitoring the change of the image on the surface of the substrate may be: measuring the change of the hue of the surface of the substrate by the chromaticity sensor embedded in the polishing table through the hole provided in the polishing pad, or measuring the surface of the substrate obtained by using the CCD. Dimension 39 320663 200936309 Method of change of imagery. A method of monitoring a change in a component (a concentration of an oxide of a by-product, and an ionity of a source derived from a conductive film) in a slurry or an electrolyte may be obtained by measuring a slurry discharged from a polishing table A method of changing the ion concentration of a conductive film. According to the present invention, in the case where there is a step on the surface of the conductive crucible, a protective film is formed in a portion above the finite value of the contact surface of the electroconductive film and the polishing pad, and the protective film is completely removed by grinding. In addition, in the conductive film and the surface of the polishing pad (4) G, the axis is insoluble in the protective film, and the protective film is not left to be polished. Thereby, in the upper stage, the conductive film is dissolved in the electrolytic solution, and the dissolution of the conductive film is suppressed in the lower portion. Therefore, the step difference of the surface of the conductive film can be quickly eliminated. ★ Next, the present invention will be described with reference to the drawings: a third embodiment. (Second Embodiment) (Substrate Processing Apparatus) The configuration of the substrate processing apparatus will be omitted from the description of the common phase of the first embodiment (5). As explained in the embodiment of the rigid face, in Fig. 2, the pressures inside the pressure chambers 21 to 25 can be independently changed by the freezer RE2 to RE6, so that the respective portions of the substrate w can be targeted. (Divided area) Adjusts the pressing force of the substrate w to the polishing crucible by the elastic 塾 (the contact surface pressure acting on the surface of the substrate). To change the tongue, as shown in Fig. 4, the pressure of each of the pressure chambers 21 to 25 is adjusted during the grinding to adjust the pressing force of the buckle 3 against the polishing crucible 101, and the substrate W is pressed to the pressing force of the polishing pad iQi. The central portion of the substrate 40 40 320663 200936309 (Fig. 4 c), and from the central portion to the intermediate portion (C2), the peripheral portion (C3), then the peripheral portion (C4), and then to the substrate w The distribution of the polishing pressure (contact surface pressure acting on the substrate surface) of each portion such as the outer peripheral portion of the outer buckle 3 is set to a desired value. Thus, the substrate W can be divided into four concentric circles and ring portions (C1 to C4)' and each portion can be pressed with an independent pressing force. Although the polishing speed is related to the pressing force of the surface to be polished of the substrate #, since the pressing force of each portion can be controlled as described above, the four portions (C1 to C4) of the base plate W can be independently controlled. Grinding speed. Therefore, even if the film thickness of the film to be honed on the surface of the substrate is unevenly distributed in the radial direction, the entire surface of the substrate W can be prevented from being insufficiently polished or excessively polished. That is, even if the film thickness of the film to be polished on the surface of the substrate w is different depending on the position in the radial direction of the substrate W, it is only necessary to make the substrate of each of the pressure chambers 21 to 25 located above The film thickness of the surface is higher than the pressure above the thick portion (4), the other pressure is high, or the pressure of the pressure chamber above the thin portion of the surface of the substrate W is lower than that of the other pressure chambers. The pressing speed of the portion to be polished on the thicker portion of the film thickness is greater than the pressing force on the surface to be polished having a thinner portion of the film thickness, so that the polishing rate of the portion can be selectively increased. Thereby, regardless of the film thickness distribution at the time of film formation, the entire surface of the polishing substrate W can be polished without excessive and insufficient. Further, in the polishing table of the present embodiment, a power supply electrode (applied to 320663 41 200936309) 264 connected to the positive electrode of the power source 252 is disposed at a position on the side of the polishing pad 1〇1. In the substrate head 1, the substrate W is brought into contact with the polishing surface in a state where a part of the substrate W is exposed on the side of the polishing pad 101, and the peripheral portion C4 of the lower surface of the substrate W is brought into contact with the feeding electrode 264. Thereby, the conductive film 66 is applied from the donor electrode 264 to the substrate W. Further, the conductive film 66 of the substrate w may be applied from the power supply electrode 264 through the buckle. Then, the support member 254 as the cathode and the conductive film on the substrate w as the anode are electrically connected by the electrolytic solution filled in the through holes 10a of the polishing pad 101. (electrolytic composite grinding method)

接著’針對本實施形態之電解複合研磨方法進行說 明。本實施形態之電解複合研磨方法之中,與第一實施形 態之電解複合研磨方法共通的部份的說明將予以省略。 第12A至12C圖係電解複合研磨之說明圖。第ι2Α至 12C圖中,作為被研磨面之導電膜66係向下配置。 首先,如第12A圖所示,一邊使電解液5〇與基板¥表 面的導電膜接觸並施加電壓至導電膜66,一邊將基板¥表 面按壓至研磨墊1〇1同時使基板?與研磨墊1〇1相對(旋轉 移動,而研磨導電膜66的表面。 因為要隔著層間絕緣膜6 2 ^疊形成複數條配線,所以 有必要以將多餘的導電膜66去除掉的狀態使基板 W的表面 平:L·化t解複合研磨就是藉由施加電屋至導電膜⑽,在 導電膜66的表面形成由電氣絕緣性物質所形成之保護 膜。形成於導電膜66的上段部Η(凹部67的外側)之保護 膜會與研磨塾101抵觸而被去除掉。因此,上段部Η的導 電膜66會溶解於電解液5〇而被去除掉。相對於此,下段 320663 42 200936309 部L(凹部67的内側)之導電膜則為保護膜所遮蔽而不會溶 解於電解液50。藉由以上之電解複合研磨,使導電膜的段 差消除掉。藉此,讓導電膜66的表面與露出的阻障膜64 的表面配置在同一平面上,而使基板W平坦化。 此處’本案之發明人發現:調整基板W表面各部位的 電位’可控制基板W的各部位的研磨速度。換言之,形成 於基板W表面的金屬膜,亦即第12A圖所示之下層的阻障 膜64與上層的導電膜66之間存在有電阻上的差異,利用 ❹此差異來調整基板W各部位的電位。從設置於金屬膜的表 面之給電電極264施加電壓至基板W的周緣部C4,在基板 W的全面都殘存有導電膜66之情況’基板的全面會具有大 致相等的電壓。不過,如第12B圖所示當導電膜66被去除 而使阻障膜64的一部分(例如給電電極264附近)露出時, 基板W表面.的電壓分佈就會變化。 具體而言,使基板W的周緣部C4區域之阻障膜64露 φ出後’基板W的周緣部C4以外的區域,亦即基板w的中心 C1至C3的區域仍有電阻比阻障膜μ小之導電膜66殘 存°因為係透過阻障膜64施加到該殘存的導電膜66,所 以施加到導電膜66的電壓會依與給電電極264的距離而降 此處,本實施形態係如第12B圖所示,首先將基板w 上之導電膜66的一部份去除而使阻障膜64露出。具體而 5 ’係〜邊控制供給至基板頭1的壓力室22至25(表照第 3圖)内的加壓流體的流量以使得基板w與研磨塾1〇1的接 320663 43 200936309 觸面壓在基板W的周緣部C4(參照第4圖)為最高,一邊進 行研磨。 至於基板W的周緣部C4以外的接觸面壓的分佈,則以 設定成從基板W的外圍部C3到中心部Cl(參照第4圖)漸 次減小之分佈為佳,不過設定成從基板W的中心部C1到夕卜 圍部C3的接觸面壓都相等亦可。 以如此之接觸面壓的分佈進行研磨,則因為在基板货 的周緣部C4的區域,亦即在給電電極264附近的區域促進 ❹研磨,所以最先去除該區域的導電膜。於是,基板W的周 緣部C4的區域之阻障膜64露出。此時,在基板W的周、緣 部C4的區域以外的區域,亦即基板W的外圍部C3到中心 部C1的區域,導電膜66仍殘存。尤其,在將基板W的接 觸面壓的分佈設定成從外圍部C3到中心部C1漸次減小之 情況,會形成為導電膜66的殘存膜厚從外圍部C3越朝向 中心部C1越厚之形態。 ©此外,將基板W上的導電膜66的一部份去除而使阻障 膜64露出之方法’還有將與基板w相向之陰極(對向電極) 分割成複數個小陰極(小電極)之使用分割陰極(分割電極) 之方法。如此之分割陰極的一個例子,有如第1 3圖所示之 分割成相對於研磨台的中心呈同心圓狀之複數個陰極K1 至K3。使最外周的陰極(第13圖之陰極^^丨與基板^^之間 的施加電壓在第7圖所示的第一變化點a的電壓以下,且 比其他的陰極ΚΙ, K2的電壓都高,則會成為與此陰極K3 相向的時間最長(頻率最高)之基板w的周緣部C4的研磨速 320663 44 200936309 •度最快之狀態,使該區域之導電膜66最先被去除。在此分 割陰極進行電壓之控制,以使得施加電壓從最外周的陰極 K3到中心的陰極K1漸漸變低(以第13圖來看的話為陰極 K3>陰極K2>陰極K1),則因為研磨會以導電膜66的殘存膜 厚從基板W的外圍部C3越朝向中心部C1越厚之狀態進 行,使阻障膜64逐漸從基板W的周緣部C4露出,所以是 不錯的一種方法。 使阻障膜64露出後,就使作用於基板W的接觸面壓的 ❿ 分佈逆轉。具體而言,係設定成使作用於基板W的周緣部 C4的接觸面壓較小、或為不接觸的狀態,使作用於基板w 的外圍部C3到中心部C1的接觸面壓較大。或者,亦可使 整個面的接觸面壓都一致。藉此,可確實防止由於機械研 磨作用所造成之磨蝕在阻障膜64露出之基板W的周緣部 C4發生。 另外,本實施形態之電解複合研磨,係一邊以膜厚感 ❹測器測量導電膜66的殘存膜厚一邊進行研磨。此膜厚感測 器最好採用渦電流感測器◦渦電流感測器係利用合成阻抗 會依各部份的膜厚而變化之現象而檢測膜厚者,且係藉由 從埋設於研磨台100内的渦電流感測器對導電膜施加高周 波而測量膜厚者。因此,即使是導電膜66 <類之膜厚較厚 的膜也可進行高精度的膜厚測量。 此處’在基板W的周緣部C4區域之阻障膜64露出, 基板W的電壓分佈發生變化之時點,提高施知於給電電極 264之電麗。具體而言,係設定成基板?的周緣部c4的區 320663 45 w ❹ ❿ 200936309 域之電壓為C點電壓以上,且 第7圖之C、D點電屋)之雷 ,、,公點電屋以上(參辟 之區域(基板W的周緣部C4區^ 障^料已露出 因此,即使基板W的周緣部 】進一步的研磨。 66,也不易在該表面形成碟形凹陷Y有配線用的導電膜 另-方面’在阻障膜64的表面 e 板w的中心部α到外有導電膜66之基 Γ固口P C3 ’電壓係通過電阻卓 障膜Θ4而施加,所以電懕 问的阻 的周緣部C4區域的電盤,> 托间基板 ^可防止有導電膜66殘存之+、 部C1到外圍部C3區域夕♦ r # 以子之中心 電流密度狀態。具體而t,在M — 士1 唯持在间 ° 係5又疋成基板W的中心部门丨 外圍部C3區域的電壓在塗7 隹第7圖之Β點電壓以下,較佳為在 ”電以下’更佳為成為d區域之電壓。 藉此基板W的周緣部C4區域就會流通例如接觸面為 0時之第一變化電壓(第7圖中之D點電壓)附近的電流’ 相對於此’基板W的中心部C1到c3區域則會流通第一變 化電壓(例如第7圖中之a點電壓)附近的 電流。換言之’ 在阻障膜64露出之區域(基板w的周緣部以區域)不會進 行進一步的研磨,而在基板f的中心部C1到C3區域則會 促進研磨。 結果’如第12C圖所示,將基板w表面之凹部63以外 的區域的導電膜去除掉。 在如上所述之本實施形態中,由於阻障膜64的露出區 域的電壓一超過臨限值電壓,電流密度就會轉而減少’所 46 320663 200936309 :;==磨速度會變低。因此,即使在阻_ 觸插塞或配線之導電歸存在之 情:,也不易在該導電膜66的表面形成 學r解作用進行研磨,所以無需如以往一 :漿—無需 _ ^ π磨所以機械研磨作用的比率降低, Γ=Γ生。再者,在阻障膜64的露出區域,研磨 ❹ 的接觸面壓變低,所以機械研磨作用的 比率降低,可防止碟形凹陷及磨蝕之發生。 F祕另二:*電阻比阻障膜64小之導電膜66殘存之 2域’電壓會因為在阻障膜64露出部份之電位下降 =’=要_電流密纽阻_64㈣㈣域高 態。因此,在導電膜66殘存之區域,研磨 =:刮痕等的損傷及碟形凹陷顺,迅速將: 盆^外’藉由使給電電極264附近的區域之接觸面壓比 =區域的接觸面壓高’使給電電極脱附近的區域 f相較於其他區域更為促進,所以會最先去除該 = 電臈66。於是,阻障骐64露出後,可在給電電極 =得到施加於金屬_電壓最高,且隨著與該 : =電壓逐漸降低之電壓分佈。因此,可在使阻障膜, 去^提馬電壓的工序中精度良好地將殘存的導電膜⑽ 第7圖中,粗線係電解液不含有會生成電氣絕緣⑷ 320663 47 200936309 • 質之添加劑的情況之曲線圖,細線表示添加了聚乙亞胺工 重量%作為會生成電氣絕緣性物質之添加劑的情況。此外, 實線係研磨墊與基板的接觸面壓為0.5 psi的情況,虚線 係接觸面壓為0 psi的情況。 已知在不含有會生成電氣絕緣性物質之添加劑(或濃 度很低)的情況,電流密度會變高。其理由可想成是因為會 生成電氣絕緣性物質之添加劑的濃度愈高愈會形成強固的 保護膜,而難以藉硏磨去除掉之緣故。因此,希望提高研 ❹磨速度時,可使用會生成電氣絕緣性物質之添加劑的濃度 低之電解液。反之,為了進行薄導電膜的研磨或進行正確 的研磨停止而希望降低研磨速度時,可使用會生成電氣絕 緣性物質之添加劑的濃度高之電解液。此外從第7圖可 头.在不含有會生成電氣絕緣性物質之添加劑(或濃^很低) 的情況,第一及第二變化電壓會變高。因此,最好依據會 生成電氣絕緣性物質之添加劑的濃度來調整施加電壓。 〇 A此外,本發明之技術範圍’並非限定於上述的實施形 態及其變形例者’而是包含在不脫離本發明宗旨的範圍内 除了上述的實施形態等之外還加上種種的變化者。亦即, 在實施形態等所舉的具體的材料及構成等只不過是一.個例 子,仍然可做適當的變化。 例如’本實施形態中,雖針對只在基板的周緣部的一 .處設置給電電極之構成進行了說明,但亦可在基板上複數 處設置給電電極。藉此’用於電壓施加的接觸面積會捭加, 可使接觸電阻削、’所以可正確地㈣提供給基板之曰電 320663 48 200936309 位。此情況,各給電電極最好設置成基板的同心圓狀。 另外’雖針對在阻障膜露出後提高電壓之構成進行了 說明,但亦可利用膜厚感測器檢測出阻障膜快露出前的那 個時點,並從那個時點開始提高電壓。 (研磨墊) 關於研磨墊的材料、形狀等,因為與第二實施形態一 樣’故將其說明予以省略。 (第四實施形態) 接著’針對本發明之電解複合研磨方法的第四實施形 態進行說明。本實施形態中,將適當援用第7圖等,且與 上述第二實施形態一樣的構成將標註相同符號而省略兑說 明。 … 、亦可使給電電極264的位置固定,而藉由使基板頭j 的位置移動來控制阻障膜64露出區域與導電膜66殘 域的電壓。 Q 使施加電壓達到稍微超過第7圖之D點的程度(〇 5v 程度),並將給電電極264(施加點)配置在很接近研磨台 1 口00的外周(距離1〇咖以内)之處。而且,在研磨初期以 只有基板W的最外周突懸之狀態進行研磨,然後在最二 的阻障膜64露出的階段使基板頭j漸漸朝離開研磨台^ 的2心之方向,亦即朝著突懸量增加之方向移動。此^, ί給電電極264 —直與阻障膜64露出的部份接觸,且蚀L 突懸的位置㈣導㈣66仍殘留之狀態。 且使未 根據如上所述之本實施形態,在阻障膜64露出的階段 320663 49 200936309 '使基板頭1漸漸朝離開硏磨台100的中心之方向移動,就 可使阻障膜64露出的區域的電壓維持在高電壓狀態。藉7 此’即使是阻障膜64的露出區域有將成為接觸插塞或配線 之導電膜66存在的情況,也不易在該導電臈66的表面形 成碟形凹陷。 ❺ 此外,亦可採用:在使基板頭1移動之後,提高施加 到給電電極264的電壓到會讓阻障膜64露出區域的電壓達 到臨限值電壓(第7圖中的C點電壓)以上之構成。 根據此構成’則即使沒有使電壓大幅上升,也可確實 地使阻障膜64露出區域的電壓達到臨限值電壓以上。藉 此,即使是阻障膜64的露出區域有將成為接觸插塞或配線 之^電膜66存在的情況,也不易在該導電*66的表面形 此外,也可確實防止阻障膜64露出的區域受 ,的研磨。因此,在導電膜66殘存區域 ❹ 所以可在抑㈣^障膜Μ露出的區域則研磨不再進行, 除導電膜66料之損傷及碟形㈣的情況下,迅速去 接觸此中,給電電極264與基板w的幾乎全體 264的材料,而日用碳樹脂等之軟質材料來作為給電電極 轉等I:對基-===之旋- 磨台⑽的夕264並不—定要位在復接近研 給電電極配置^處。例如’也可在研磨塾4内將電應之 5心圓狀。在此一情況,即使使基板诼緩 320663 50 200936309 •緩地向外側移動,也能以基板w不突懸的狀態進行研磨β 以上針對給電電極264配置在很接近研磨台1〇〇的外 周(距離10 mm以内)之處的情況進行了說明,惟亦可在研 磨塾4埋設例如1 cm左右寬度的同心圓狀的導電性塾,來 作為給電電極的另外的實施例。將導電性墊配置在與研磨 台101外周的距離大於基板W的半徑之内側的位置,則即 使導電性墊到達基板的中心也能以基板W不突懸的狀態穩 定地進行研磨。 ❹ 根據本發明,底膜的露出區域的電壓係設定成超過臨 限值電壓,藉此’即使在底膜的露出區域有將成為接觸插 塞或配線之導電膜存在的情況,也不易在該導電膜的表面 形成碟形凹陷。另外,因為利用電化學性的溶解作用進行 研磨,所以無需如以往一樣使用高磨粒濃度的研磨漿,且 無需以·高接觸面壓進行研磨,所以機械研磨作用的比率降 低,可防止磨钱之發生。 另一方面,在電阻比底膜小之導電膜仍殘存之區域, 電壓係設定成超過臨限值電壓且在前述最大電壓以下,藉 此使該區域在研磨到與底膜相同水平而平坦化之前都維持 高電流密度狀態。因此,即使在有將成為接觸插塞或配線 之導電膜存在的情況,研磨也會繼續進行,所以可在抑制 刮痕等之損傷及碟形凹陷的情況下,迅速去除導電膜而達 到平坦化。 以上,已針對本發明之較佳的實施例進行了說明,惟 本發明並不限定於這些實施例。在不脫離本發明的宗旨之 51 320663 200936309 範圍内,仍可有構成之附加、省略、置換,以及其他的變 更。本發明並不受前述的說明所限定,僅受隨附之申請專 利範圍所載的範圍所限定。 【圖式簡單說明】 第1圖係顯示基板處理裝置的配置構成之平面圖。 第2圖係電解複合研磨裝置之概略構成圖。 第3圖係基板頭之斷面圖。 第4圖係基板頭之底面圖。 ❹ 第5A圖係概略地顯示電解複合研磨裝置的重要部份 之縱斷面圖。 第5B圖係概略地顯示電解複合研磨裝置的重要部份 之縱斷面圖。 第6A圖係電解複合研磨之說明圖。 - 第6B圖係電解複合研磨之說明圖。 第6C圖係電解複合研磨之說明圖。 第7圖係顯示導電膜的電位與電流密度的關係之曲線Next, the electrolytic composite polishing method of the present embodiment will be described. In the electrolytic composite polishing method of the present embodiment, the description of the portions common to the electrolytic composite polishing method of the first embodiment will be omitted. Figures 12A to 12C are explanatory views of electrolytic composite grinding. In the figures 1 to 12C, the conductive film 66 as the surface to be polished is disposed downward. First, as shown in Fig. 12A, while the electrolyte solution 5 is brought into contact with the conductive film on the surface of the substrate and a voltage is applied to the conductive film 66, the surface of the substrate is pressed against the polishing pad 1〇1 while the substrate is being formed. It is opposite to the polishing pad 1〇1 (rotational movement, and the surface of the conductive film 66 is polished. Since a plurality of wirings are formed by laminating the interlayer insulating film 6 2, it is necessary to remove the excess conductive film 66 in a state of being removed. The surface of the substrate W is flat: L·Chemical de-composite polishing is to form a protective film formed of an electrically insulating substance on the surface of the conductive film 66 by applying a house to the conductive film (10). The upper portion of the conductive film 66 is formed. The protective film of the crucible (the outer side of the concave portion 67) is removed by the contact with the polishing crucible 101. Therefore, the conductive film 66 of the upper portion is dissolved in the electrolytic solution 5, and is removed. In contrast, the lower portion 320663 42 200936309 The conductive film of the portion L (inside of the concave portion 67) is shielded by the protective film and is not dissolved in the electrolytic solution 50. By the above electrolytic composite polishing, the step of the conductive film is eliminated. Thereby, the conductive film 66 is made The surface is disposed on the same plane as the surface of the exposed barrier film 64, and the substrate W is planarized. Here, the inventors of the present invention have found that adjusting the potential of each portion of the surface of the substrate W can control the polishing of each portion of the substrate W. speed. In other words, there is a difference in resistance between the metal film formed on the surface of the substrate W, that is, the barrier film 64 of the lower layer shown in FIG. 12A and the conductive film 66 of the upper layer, and the difference between the portions of the substrate W is adjusted by using the difference. When a voltage is applied from the power supply electrode 264 provided on the surface of the metal film to the peripheral portion C4 of the substrate W, and the conductive film 66 remains in the entire surface of the substrate W, the entire substrate will have substantially equal voltages. However, When the conductive film 66 is removed to expose a portion of the barrier film 64 (for example, in the vicinity of the power supply electrode 264) as shown in Fig. 12B, the voltage distribution of the surface of the substrate W changes. Specifically, the periphery of the substrate W is made. In the region other than the peripheral portion C4 of the substrate W after the barrier film 64 in the portion C4 is exposed, the region of the center C1 to C3 of the substrate w remains as the conductive film 66 having a smaller resistance than the barrier film μ. The resist film 64 is applied to the remaining conductive film 66. Therefore, the voltage applied to the conductive film 66 is lowered depending on the distance from the power supply electrode 264. In this embodiment, as shown in FIG. 12B, the substrate is first introduced. Conductive film 66 on w Partial removal causes the barrier film 64 to be exposed. Specifically, the 5' system side controls the flow rate of the pressurized fluid supplied to the pressure chambers 22 to 25 of the substrate head 1 (refer to FIG. 3) so that the substrate w and the polishing 6631〇1 is connected to 320663 43 200936309 The contact surface is pressed to the highest edge portion C4 (see Fig. 4) of the substrate W, and is polished. The distribution of the contact surface pressure other than the peripheral edge portion C4 of the substrate W is set. It is preferable that the distribution gradually decreases from the outer peripheral portion C3 of the substrate W to the central portion C1 (see FIG. 4), but the contact surface pressure from the central portion C1 of the substrate W to the outer peripheral portion C3 is set to be equal. When the polishing is performed in such a manner as to contact the surface pressure, the conductive film is removed first in the region of the peripheral portion C4 of the substrate, that is, in the region near the feeding electrode 264. Then, the barrier film 64 in the region of the peripheral portion C4 of the substrate W is exposed. At this time, in the region other than the region of the substrate W and the edge portion C4, that is, the region from the peripheral portion C3 of the substrate W to the central portion C1, the conductive film 66 remains. In particular, when the distribution of the contact surface pressure of the substrate W is set to gradually decrease from the outer peripheral portion C3 to the central portion C1, the residual film thickness of the conductive film 66 is formed to be thicker from the outer peripheral portion C3 toward the central portion C1. form. Further, the method of removing a portion of the conductive film 66 on the substrate W to expose the barrier film 64 is further divided into a plurality of small cathodes (small electrodes) which are opposed to the substrate w (opposing electrode) A method of dividing a cathode (dividing electrode) is used. An example of such a divided cathode is a plurality of cathodes K1 to K3 which are divided into concentric circles with respect to the center of the polishing table as shown in Fig. 13. The voltage applied between the cathode of the outermost periphery (the cathode of Fig. 13 and the substrate) is lower than the voltage of the first change point a shown in Fig. 7, and the voltage of K2 is higher than that of the other cathodes When it is high, the polishing speed 32062 44 200936309 of the peripheral portion C4 of the substrate w having the longest (highest frequency) direction with respect to the cathode K3 is the fastest, and the conductive film 66 in this region is removed first. The divided cathode performs voltage control such that the applied voltage gradually decreases from the outermost peripheral cathode K3 to the central cathode K1 (the cathode K3 > cathode K2 > cathode K1 as seen in Fig. 13), because the grinding The remaining film thickness of the conductive film 66 is made thicker from the outer peripheral portion C3 of the substrate W toward the central portion C1, and the barrier film 64 is gradually exposed from the peripheral edge portion C4 of the substrate W. Therefore, it is a good method. After the film 64 is exposed, the ❿ distribution of the contact surface pressure acting on the substrate W is reversed. Specifically, the contact surface pressure acting on the peripheral edge portion C4 of the substrate W is set to be small or not in contact with each other. Acting on the peripheral portion C3 of the substrate w to the middle The contact surface pressure of the core portion C1 is large. Alternatively, the contact surface pressure of the entire surface can be made uniform. Thereby, it is possible to surely prevent the abrasion caused by the mechanical polishing action on the peripheral portion of the substrate W exposed by the barrier film 64. In addition, in the electrolytic composite polishing of the present embodiment, polishing is performed while measuring the residual film thickness of the conductive film 66 by a film thickness detector. The film thickness sensor preferably uses an eddy current sensor vortex. The current sensor detects the film thickness by a phenomenon in which the combined impedance changes depending on the film thickness of each portion, and is measured by applying a high frequency to the conductive film from an eddy current sensor embedded in the polishing table 100. Therefore, even a film having a thick film thickness of the conductive film 66 can be subjected to high-accuracy film thickness measurement. Here, the barrier film 64 in the peripheral portion C4 region of the substrate W is exposed, and the substrate is exposed. When the voltage distribution of W changes, the electric power applied to the power supply electrode 264 is increased. Specifically, the area of the peripheral portion c4 of the substrate is set to 320663 45 w ❹ ❿ 200936309 The voltage of the domain is equal to or higher than the C point voltage. And points C and D in Figure 7 The thunder of the electric house, and the above-mentioned electric house (the area to be inspected (the C4 area of the substrate W is exposed, so even the peripheral portion of the substrate W) is further polished. 66, it is not easy to The surface is formed with a dish-shaped recess Y having a conductive film for wiring. On the surface of the barrier film 64, the central portion α of the plate w to the base of the outer conductive film 66 is fixed to the voltage P C3 '. Since the barrier film 4 is applied, the electric disk of the peripheral portion C4 region of the electric resistance is prevented, and the inter-substrate substrate can prevent the remaining portion of the conductive film 66, the portion C1, and the peripheral portion C3 region. Central current density state. Specifically, in the case where M_士1 is only in the center portion 5 and is formed in the central portion of the substrate W, the voltage in the peripheral portion C3 is below the voltage at the point 7 of Fig. 7, preferably "electricity". In the following, it is more preferable to be the voltage in the d region. Thereby, the region around the peripheral portion C4 of the substrate W flows, for example, the current in the vicinity of the first varying voltage (voltage at point D in FIG. 7) when the contact surface is 0. In the central portion C1 to c3 of the 'substrate W, a current near the first varying voltage (for example, the voltage at point a in FIG. 7) flows. In other words, the region where the barrier film 64 is exposed (the peripheral portion of the substrate w is The region is not subjected to further polishing, and the polishing is promoted in the central portions C1 to C3 of the substrate f. As a result, as shown in Fig. 12C, the conductive film in the region other than the concave portion 63 on the surface of the substrate w is removed. In the present embodiment as described above, since the voltage of the exposed region of the barrier film 64 exceeds the threshold voltage, the current density is decreased by '46 320663 200936309 :; == the grinding speed is lowered. Even if the resistance of the resist _ plug or wiring is present : It is also difficult to form a polishing solution on the surface of the conductive film 66, so that it is not necessary to use a conventional slurry: the ratio of the mechanical polishing action is lowered, and the ratio of the mechanical polishing action is lowered. In the exposed area of the barrier film 64, the contact surface pressure of the polishing crucible becomes low, so the ratio of the mechanical polishing action is lowered, and dishing and abrasion can be prevented. F secret 2: * Resistive film having a smaller resistance than the barrier film 64 The remaining 2 domain 'voltage will drop due to the potential drop in the exposed portion of the barrier film 64 = '= _ current dense resistance _64 (four) (four) domain high state. Therefore, in the region where the conductive film 66 remains, the grinding =: scratch If the damage and the dishing are smooth, the basin will be replaced by the contact surface pressure ratio of the region near the feeding electrode 264 = the contact surface of the region is high, so that the region f near the feeding electrode is compared with the other The area is more promoted, so the first = 臈 66 is removed. Therefore, after the barrier 骐 64 is exposed, the voltage applied to the metal _ can be obtained at the power supply electrode, and the voltage is gradually lowered with the voltage of : Distribution. Therefore, it is possible to make the barrier film In the step of the horse voltage, the remaining conductive film (10) is accurately placed. In the seventh figure, the thick-line electrolyte does not contain a graph showing the case where electrical insulation is generated (4) 320663 47 200936309 • The thin line indicates that polyethylene is added. The weight of the imiline is used as an additive which generates an electrically insulating substance. In addition, the contact pressure of the solid line between the polishing pad and the substrate is 0.5 psi, and the line pressure of the broken line is 0 psi. In the case where the additive (or the concentration is low) which generates an electrically insulating substance is not contained, the current density becomes high. The reason is conceivable because the higher the concentration of the additive which generates the electrically insulating substance, the stronger the stronger. The film is protected and it is difficult to remove it by honing. Therefore, when it is desired to increase the honing speed, an electrolyte having a low concentration of an additive which generates an electrically insulating substance can be used. On the other hand, in order to reduce the polishing rate in order to polish the thin conductive film or to stop the correct polishing, an electrolyte having a high concentration of an additive which generates an electrically insulating substance can be used. Further, it can be seen from Fig. 7. The first and second varying voltages become high without containing an additive (or a low concentration) which generates an electrically insulating substance. Therefore, it is preferable to adjust the applied voltage in accordance with the concentration of the additive which generates the electrically insulating substance. Further, the technical scope of the present invention is not limited to the above-described embodiments and modifications thereof, but includes various modifications in addition to the above-described embodiments and the like without departing from the scope of the present invention. . That is, the specific materials, configurations, and the like given in the embodiments and the like are merely examples, and appropriate changes can be made. For example, in the present embodiment, the configuration in which the feeding electrode is provided only at one of the peripheral portions of the substrate has been described. However, the feeding electrode may be provided in plural places on the substrate. Thereby, the contact area for voltage application is increased, and the contact resistance can be cut, so that the substrate can be correctly supplied to the substrate 320663 48 200936309. In this case, each of the feeding electrodes is preferably provided in a concentric shape of the substrate. Further, although the configuration for increasing the voltage after the barrier film is exposed has been described, the film thickness sensor can be used to detect the time before the barrier film is exposed, and the voltage is raised from that point in time. (Polishing pad) The material, shape and the like of the polishing pad are the same as those of the second embodiment, and the description thereof will be omitted. (Fourth embodiment) Next, a fourth embodiment of the electrolytic composite polishing method of the present invention will be described. In the present embodiment, the same reference numerals are given to the same components as those in the second embodiment, and the description thereof will be omitted. The position of the power supply electrode 264 can also be fixed, and the voltage of the exposed region of the barrier film 64 and the residual region of the conductive film 66 can be controlled by moving the position of the substrate head j. Q The applied voltage is slightly above the point D of Fig. 7 (〇5v), and the feeding electrode 264 (applying point) is placed very close to the outer circumference of the grinding station 1 00 (within 1 〇 coffee) . Further, at the initial stage of polishing, polishing is performed in a state in which only the outermost periphery of the substrate W is suspended, and then the substrate head j gradually moves away from the center of the polishing table 2 at the stage where the second barrier film 64 is exposed, that is, toward Move in the direction of increasing the amount of suspension. The voltage of the electrode 264 is in direct contact with the exposed portion of the barrier film 64, and the position (4) of the etched L is still remaining. Further, according to the present embodiment as described above, in the stage where the barrier film 64 is exposed 320663 49 200936309 'the substrate head 1 is gradually moved away from the center of the honing table 100, the barrier film 64 can be exposed. The voltage of the region is maintained at a high voltage state. By the fact that even in the exposed region of the barrier film 64, there is a case where the conductive film 66 which becomes a contact plug or wiring exists, it is difficult to form a dish-shaped recess on the surface of the conductive crucible 66. Further, after the substrate head 1 is moved, the voltage applied to the power supply electrode 264 may be increased until the voltage at which the barrier film 64 is exposed reaches a threshold voltage (voltage C at the seventh point). The composition. According to this configuration, even if the voltage is not largely increased, the voltage in the region where the barrier film 64 is exposed can be surely brought to a threshold voltage or higher. Thereby, even if the exposed region of the barrier film 64 has the electric film 66 to be a contact plug or a wiring, it is difficult to form the surface of the conductive film 66, and the barrier film 64 can be surely prevented from being exposed. The area is affected by the grinding. Therefore, in the remaining region of the conductive film 66, the polishing may not be performed in the region where the barrier film is exposed, and in the case of the damage of the conductive film 66 and the dish shape (4), the contact is quickly contacted, and the power supply electrode is provided. 264 and almost all of the material 264 of the substrate w, and a soft material such as a daily carbon resin is used as the power feeding electrode, etc. I: the base-=== spin-milling station (10) is not necessarily located at The structure is close to the electric electrode configuration. For example, it is also possible to make the electric heart 5 in the grinding crucible 4. In this case, even if the substrate is relieved by 320663 50 200936309, the substrate w can be polished without being overhanged. The power supply electrode 264 is disposed on the outer periphery of the polishing table 1〇〇. Although the case where the distance is within 10 mm is described, a concentric circular conductive crucible having a width of, for example, about 1 cm may be embedded in the polishing crucible 4 as another embodiment of the feeding electrode. When the conductive pad is disposed at a position larger than the outer circumference of the polishing table 101 by a distance larger than the radius of the substrate W, even if the conductive pad reaches the center of the substrate, the substrate W can be stably ground without being suspended. According to the present invention, the voltage of the exposed region of the under film is set to exceed the threshold voltage, whereby it is difficult to use the conductive film to be a contact plug or a wiring even in the exposed region of the under film. The surface of the conductive film forms a dishing recess. Further, since the polishing is performed by the electrochemical dissolution action, it is not necessary to use a polishing slurry having a high abrasive grain concentration as in the related art, and it is not necessary to perform polishing with a high contact surface pressure, so that the ratio of the mechanical polishing action is lowered, and the grinding money can be prevented. It happened. On the other hand, in a region where the electric resistance of the conductive film smaller than the base film remains, the voltage is set to exceed the threshold voltage and is lower than the maximum voltage, thereby planarizing the region to the same level as the base film. The high current density state was maintained before. Therefore, even if there is a conductive film to be a contact plug or a wiring, the polishing is continued, so that the conductive film can be quickly removed and flattened while suppressing damage such as scratches and dishing. . The preferred embodiments of the present invention have been described above, but the present invention is not limited to the embodiments. Additions, omissions, substitutions, and other modifications can be made without departing from the scope of the invention. The invention is not limited by the foregoing description, but is only limited by the scope of the appended claims. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a plan view showing the arrangement of a substrate processing apparatus. Fig. 2 is a schematic configuration diagram of an electrolytic composite polishing apparatus. Figure 3 is a cross-sectional view of the substrate head. Figure 4 is a bottom view of the substrate head. ❹ Fig. 5A is a longitudinal sectional view showing an important part of the electrolytic composite polishing apparatus. Fig. 5B is a longitudinal sectional view schematically showing an important part of the electrolytic composite polishing apparatus. Fig. 6A is an explanatory view of electrolytic composite polishing. - Figure 6B is an explanatory diagram of electrolytic composite grinding. Fig. 6C is an explanatory view of electrolytic composite polishing. Figure 7 shows the relationship between the potential of the conductive film and the current density.

第8A圖係施加各區域的電壓時之保護膜形成狀態之 說明圖,此圖顯示α區域之情形。 第8Β圖係施加各區域的電壓時之保護膜形成狀態之 說明圖,此圖顯示冷區域之情形。 第8C圖係施加各區域的電壓時之保護膜形成狀態之 說明圖’此圖顯不7區域之情形。 第9圖係顯示使電解液的pH變化時之施加電壓輿電流 52 320663 200936309 密度的關係之曲線圖。 第ίο圖係顯示使研磨墊的轉速變化時之施加電壓與 電流密度的關係之曲線圖。 第11圖係概略地顯示化學機械研磨裝置的重要部份 之縱斷面圖。 第12A圖係電解複合研磨之說明圖。 第12B圖係電解複合研磨之說明圖。 第12C圖係電解複合研磨之說明圖。 ❹ 第13圖係顯示研磨台的其他構成之平面圖。 【主要元件符號說明】 1 基板頭 2 基板頭本體 2a 殼體部 2b 加壓片支持部 2c 密封部 2d 凹部 3 扣環 4· 彈性墊 5 保持壞 5a 上端部 5b 檔止部 6 爽持板 7 加壓片 8 中央袋 9 環形管 10 萬向接頭部 11 基板頭驅動軸 11a 凹部 12 轴承球 21 至 25 壓力室 31, 33至36 流路 41 開口部 42 凸部 43 流路 50 電解液 52 研磨漿 55, 56 螺絲 62 層間絕緣膜 53 320663 200936309Fig. 8A is an explanatory view showing a state in which a protective film is formed when a voltage of each region is applied, and this figure shows a case of an α region. Fig. 8 is an explanatory view showing a state in which a protective film is formed when a voltage of each region is applied, and this figure shows a case of a cold region. Fig. 8C is an explanatory view showing the state of formation of a protective film when voltages of respective regions are applied. This figure shows the case of 7 regions. Fig. 9 is a graph showing the relationship between the applied voltage 舆 current 52 320663 200936309 density when the pH of the electrolyte is changed. Fig. ίο is a graph showing the relationship between the applied voltage and the current density when the rotational speed of the polishing pad is changed. Fig. 11 is a longitudinal sectional view schematically showing an important part of the chemical mechanical polishing apparatus. Fig. 12A is an explanatory view of electrolytic composite polishing. Fig. 12B is an explanatory view of electrolytic composite polishing. Fig. 12C is an explanatory view of electrolytic composite polishing. ❹ Fig. 13 is a plan view showing another configuration of the polishing table. [Description of main component symbols] 1 substrate head 2 substrate head body 2a housing portion 2b pressure piece support portion 2c sealing portion 2d recess portion 3 buckle 4 Pressure piece 8 Central pocket 9 Annular tube 10 Universal joint part 11 Substrate head drive shaft 11a Recessed part 12 Bearing ball 21 to 25 Pressure chamber 31, 33 to 36 Flow path 41 Opening portion 42 Projection portion 43 Flow path 50 Electrolyte 52 Grinding Pulp 55, 56 screw 62 interlayer insulation film 53 320663 200936309

63, 67 凹部 64 66 導電膜 70 至 72 81, 91 彈性膜 82 82a, 92a 螺絲孔 92 100 研磨台 101 101a 貫通孔 102 102a 供給口 110 111 基板頭用氣缸 112 113’ 116時規滑輪 114 115 時規皮帶 117 120 壓縮空氣源 121 200 走行機構 202, 208 204 基板IE 206 210 旋轉輸送器 212 214 洗淨單元 218 222 水槽 224, 226 228 感測器線圈 250 252 電源 254 254a 蓋件 254b 255 連通孔 256 258A 第一電解液接受口 258B 262 電氣接點 264 300 基板處理裝置 310 Cl 中心部 C2 組障臈 保護膜 +央袋保持件 環形管保持件 研磨塾 電解液供給喷嘴 擺動臂 旋轉筒 基板頭用馬達 轴63, 67 concave portion 64 66 conductive film 70 to 72 81, 91 elastic film 82 82a, 92a screw hole 92 100 polishing table 101 101a through hole 102 102a supply port 110 111 substrate head cylinder 112 113' 116 timing pulley 114 115 Gauge belt 117 120 compressed air source 121 200 travel mechanism 202, 208 204 substrate IE 206 210 rotary conveyor 212 214 cleaning unit 218 222 sink 224, 226 228 sensor coil 250 252 power supply 254 254a cover 254b 255 communication hole 256 258A first electrolyte receiving port 258B 262 electrical contact 264 300 substrate processing device 310 Cl central portion C2 group barrier protective film + central bag holder annular tube holder grinding 塾 electrolyte supply nozzle oscillating arm rotating cylinder substrate head motor axis

真空源 搬送機器人 基板站 乾燥單元 修整器 ITM 電解複合研磨裝置 支持構件 底件 連通溝 第二電解液接受口 給電電極 控制部 中間部 320663 54 200936309 C3 外圍部 C4 Η 上段部 L Κ1 至 Κ3 陰極 RE1 W 基板 周緣部 下段部 RE6 調節器Vacuum source transfer robot substrate station Drying unit trimmer ITM Electrolytic composite grinding device support member bottom member communication groove second electrolyte receiving port power supply electrode control portion intermediate portion 320663 54 200936309 C3 peripheral portion C4 上 upper segment L Κ1 to Κ3 cathode RE1 W Sub-section peripheral portion RE6 regulator

❹ 55 320663❹ 55 320663

Claims (1)

200936309 七、申請專利範圍: 1. 一種電解複合研磨方法,係藉由一邊使電解液與形成於 基板表面的導電膜接觸並施加電壓至前述導電膜,一邊 以預定的接觸面壓將前述基板表面按壓至研磨墊同時 使前述基板與前述研磨墊相對移動,而研磨前述導電膜 的表面之電解複合研磨方法,其特徵在於: 前述電解液係pH 4至10者,且 以在使前述接觸面壓為0之狀態使前述電壓增加 @ 時,電流密度從增加轉為減少之電壓作為最小電壓, 以在使前述接觸面壓為有限值之狀態使前述電壓 增加時,電流密度從增加後之減少轉為不再減少之電壓 作為最大電壓, 而一邊將前述電壓維持在前述最小電壓以上且前 述最大電壓以下,一邊研磨前述導電膜的表面。. 2. —種電解複合研磨方法,係藉由一邊使電解液與形成於 基板表面的導電膜接觸並施加電壓至前述導電膜,一邊 ® 以預定的接觸面壓將前述基板表面按壓至研磨墊同時 使前述基板與前述研磨塾相對移動,而研磨前述導電膜 的表面之電解複合研磨方法,其特徵在於: 前述電解液係pH 4至10者,且 以在使前述接觸面壓為0之狀態使前述電壓增加 時,電流密度從增加轉為減少之電壓作為最小電壓, 以在使前述接觸面壓為有限值之狀態使前述電壓 增加時,電流密度從增加轉為減少之電壓作為最大電 56 320663 200936309 壓, 而一邊將前述電壓維持在前述最小電壓以上且前 述最大電壓以下,一邊研磨前述導電膜的表面。 3. 如申請專利範圍第1項或第2項之電解複合研磨方法, 其中,藉由調整前述電解液之pH而控制前述導電膜的 研磨速度。 4. 如申請專利範圍第1項或第2項之電解複合研磨方法, 其中,前述電解液包含會與前述導電膜反應而生成電氣 ❿ 絕緣性物質之添加劑,且藉由調整前述添加劑的濃度而 控制前述導電膜的研磨速度。 5. 如申請專利範圍第1項或第2項之電解複合研磨方法, 其中,藉由調整前述研磨墊的轉速而控制前述導電膜的 研磨速度。 6. 如申請專利範圍第1項或第2項之電解複合研磨方法, 其中.,前述導電膜係為鎢膜。 7. —種研磨方法,係具有一邊以預定的接觸面壓將基板表 面按壓至研磨墊一邊使前述基板與前述研磨墊相對移 動,而研磨形成於前述基板表面的導電膜之研磨工序, 其特徵在於具有保護膜形成工序,此保護膜形成工序 係: 以在一邊使前述基板與前述研磨墊相對移動一邊 .使前述接觸面壓為0的狀態,使電解液與前述導電膜接 觸同時施加電壓並使該電壓增加時,電流密度從增加後 之減少轉為不再減少之電壓作為臨限值電壓, 57 320663 200936309 且在前述研磨工序之前,在使前述基板與前述研磨 墊並不接觸之狀態,使電解液與前述導電膜接觸同時施 加前述臨限值電壓以上的電壓,而在前述導電膜的表面 形成保護膜。 8. 如申請專利範圍第7項之研磨方法,其中,前述研磨工 序係為化學機械研磨工序或電解複合研磨工序。 9. 如申請專利範圍第7項或第8項之研磨方法,其中,前 述導.電膜係為鶴膜。 ❿ 10. —種電解複合研磨方法,係藉由一邊使電解液與形成於 基板表面的金屬膜接觸並施加電壓至前述金屬膜,一邊 以預定的接觸面壓將前述基板表面按壓至研磨墊同時 使前述基板與前述研磨墊相對移動,而研磨前述金屬膜 的表面之電解複合研磨方法,其特徵在: •前述電解液係pH 4至10者,前述金屬膜係由下層 之底膜及電阻比該底膜小之上層的導電膜所構成, 該電解複合研磨方法具有: 先去除前述電壓的施加點附近的前述導電膜而使 前述底膜露出之工序、以及 在前述底膜快露出或露出後提高前述電壓之工序, 提高前述電壓之工序係: 以在使前述基板與前述研磨塾相對移動同時使前 述接觸面壓為0的狀態提高前述電壓時,電流密度從增 加轉為減少之電壓作為臨限值電壓, 而提高前述電壓到使得前述底膜露出區域之電壓 58 320663 200936309 超過前述臨限值電壓。 11. 如申請專利範圍第10項之電解複合研磨方法,其中, 提高前述電壓之工序係: 以在使前述接觸電壓為有限值之狀態提高前述電 壓時,電流密度從增加後減少轉為不再減少之電壓作為 最大電壓, 而提高前述電壓到使得前述底膜露出區域以外的 區域之電壓超過前述臨限值電壓且在前述最大電壓以 ❿下。 12. 如申請專利範圍第10項之電解複合研磨方法,其中, 使前述底膜露出之工序,係使前述施加點附近的區域中 之前述基板與前述研磨塾之前述接觸面壓,比前述施加 .點附近的區域以外的區域中之前述接觸面壓高。 13. 如申請專利範圍第10項之電解複合研磨方法,其中, 使前述底膜露出之工序係: 使與前述基板相向之對向電極,成為由在同一平面 上呈同心圓狀配置之複數個小電極所構成之分割電極, 且控制前述分割電極的前述電壓,以使與前述基板 的外側部相向的頻率較高的順序使得研磨速度變快。 14. 如申請專利範圍第10項之電解複合研磨方法,其中, 係一邊以渦電流方式測量前述導電膜的殘存膜厚一邊 進行研磨。 15. 如申請專利範圍第10項之電解複合研磨方法,其中, 前述導電膜係為鎮膜。 59 320663 200936309 16. —種電解複合研磨方法,係藉由一邊使電解液與形成於 基板表面的金屬膜接觸並施加電壓至前述金屬膜,一邊 以預定的接觸面壓將前述基板表面按壓至研磨墊同時 使前述基板與前述研磨墊相對移動,而研磨前述金屬膜 的表面之電解複合研磨方法,其特徵在: 前述電解液係pH 4至10者,前述金屬膜係由下層 之底膜及電阻比該底膜小之上層的導電膜所構成, 該電解複合研磨方法具有: ® 將前述電壓之施加點配置於前述基板的周緣部而 先去除周緣部的前述導電膜使前述底膜露出之工序、以 及 在談工序之後使前述電壓之施加點從基板的周緣 部向中心部移動而使前述底膜露出之工序。 17. —種電解複合研磨方法,係藉由一邊使電解液與形成於 基板表面的金屬膜接觸並施加電壓至前述金屬膜,一邊 以預定的接觸面壓將前述基板表面按壓至研磨墊同時 ® 使前述基板與前述研磨墊相對移動,而研磨前述金屬膜 的表面之電解複合研磨方法,其中, 前述電解液係pH 4至10者,前述金屬膜係由下層 之底膜及電阻比該底膜小之上層的導電膜所構成, 該電解複合研磨方法具有: 將前述電壓之施加點配置於前述基板的周緣部而 先去除該周緣部的前述導電膜使前述底膜露出之工序、 在該工序之後使前述電壓之施加點從前述基板的 60 320663 200936309 周緣部向中心部移動而使前述底膜露出之工序、以及 在前述底膜快露出或露出後提高前述電壓之工序, 提高前述電壓之工序係: 以在使前述基板與前述研磨墊相對移動同時使前 述接觸面壓為〇的狀態提高前述電壓時,電流密度從增 加轉為減少之電壓作為臨限值電壓,而提高前述電壓到 使得前述底膜露出區域之電壓超過前述臨限值電壓。 18. 如申請專利範圍第1或第2項之電解複合研磨方法,其 ❹ 中,施加至前述導電膜之電壓係正的電壓。 19. 如申請專利範圍第7項之研磨方法,其中,施加至前述 導電膜之電壓係正的電壓。 61 320663200936309 VII. Patent application scope: 1. An electrolytic composite grinding method is to press the substrate surface with a predetermined contact surface pressure by contacting the electrolyte with a conductive film formed on the surface of the substrate and applying a voltage to the conductive film. An electrolytic composite polishing method of pressing the polishing pad while moving the substrate and the polishing pad to polish the surface of the conductive film, wherein the electrolyte is at a pH of 4 to 10, and the contact surface is pressed When the voltage is increased to @ by the state of 0, the voltage whose current density is changed from the increase to the decrease is taken as the minimum voltage, and when the voltage is increased in a state where the contact surface pressure is a finite value, the current density is decreased from the increase. The surface of the conductive film is polished while maintaining the voltage at a voltage not lower than the minimum voltage and the maximum voltage or lower. 2. An electrolytic composite polishing method in which a surface of the substrate is pressed to a polishing pad with a predetermined contact surface pressure by bringing an electrolyte into contact with a conductive film formed on a surface of the substrate and applying a voltage to the conductive film. An electrolytic composite polishing method for simultaneously polishing the surface of the conductive film while moving the substrate and the polishing pad, wherein the electrolyte is at a pH of 4 to 10, and the contact surface is pressed to a pressure of 0. When the voltage is increased, the voltage whose current density is changed from the increase to the decrease is taken as the minimum voltage, and when the voltage is increased in a state where the contact surface pressure is a finite value, the current density is changed from the increase to the decrease voltage as the maximum power. 320663 200936309 The surface of the conductive film is polished while maintaining the voltage above the minimum voltage and below the maximum voltage. 3. The electrolytic composite polishing method according to claim 1 or 2, wherein the polishing rate of the conductive film is controlled by adjusting the pH of the electrolyte. 4. The electrolytic composite polishing method according to claim 1 or 2, wherein the electrolytic solution contains an additive which reacts with the conductive film to form an electrical insulating material, and adjusts the concentration of the additive. The polishing rate of the aforementioned conductive film is controlled. 5. The electrolytic composite polishing method according to claim 1 or 2, wherein the polishing rate of the conductive film is controlled by adjusting a rotation speed of the polishing pad. 6. The electrolytic composite polishing method according to claim 1 or 2, wherein the conductive film is a tungsten film. 7. A polishing method of polishing a conductive film formed by polishing a substrate formed on a surface of the substrate while pressing a substrate surface to a polishing pad with a predetermined contact surface pressure to move the substrate and the polishing pad. In the protective film forming step, the protective film forming step is performed by moving the electrolyte to the conductive film while applying a voltage while moving the substrate and the polishing pad relative to each other. When the voltage is increased, the current density is changed from the increased decrease to the voltage that is no longer reduced as the threshold voltage, 57 320663 200936309, and before the grinding process, the substrate is not in contact with the polishing pad, A protective film is formed on the surface of the conductive film by bringing the electrolytic solution into contact with the conductive film while applying a voltage equal to or higher than the threshold voltage. 8. The polishing method according to claim 7, wherein the polishing step is a chemical mechanical polishing step or an electrolytic composite polishing step. 9. The method of claim 7, wherein the conductive film is a crane film. ❿ 10. An electrolytic composite polishing method in which a surface of the substrate is pressed to a polishing pad at a predetermined contact surface pressure while bringing an electrolytic solution into contact with a metal film formed on a surface of the substrate and applying a voltage to the metal film. An electrolytic composite polishing method for polishing a surface of the metal film by relatively moving the substrate and the polishing pad, wherein: the electrolyte solution has a pH of 4 to 10, and the metal film is a bottom film and a resistance ratio of the lower layer. The electroconductive composite polishing method comprises: a step of removing the conductive film in the vicinity of an application point of the voltage, exposing the underlying film, and exposing or exposing the underlying film; In the step of increasing the voltage, the step of increasing the voltage is to increase the current density from an increase to a decrease when the substrate is moved relative to the polishing crucible while the contact surface pressure is zero. Limiting the voltage, and increasing the voltage to the voltage of the exposed area of the underlying film 58 320663 200936309 Exceed the aforementioned threshold voltage. 11. The electrolytic composite polishing method according to claim 10, wherein the step of increasing the voltage is: when the voltage is increased in a state where the contact voltage is a finite value, the current density is decreased from increasing to no longer The reduced voltage is used as the maximum voltage, and the voltage is increased so that the voltage of the region outside the exposed region of the underlying film exceeds the threshold voltage and is at the maximum voltage. 12. The electrolytic composite polishing method according to claim 10, wherein the step of exposing the under film is to press the contact surface between the substrate and the polishing pad in a region in the vicinity of the application point, as compared with the application The aforementioned contact surface pressure in the region other than the region near the point is high. 13. The electrolytic composite polishing method according to claim 10, wherein the step of exposing the underlayer is such that a counter electrode facing the substrate is a plurality of concentrically arranged on the same plane The divided electrode formed by the small electrode controls the voltage of the split electrode so that the frequency of the opposite direction to the outer portion of the substrate is higher, so that the polishing speed is increased. 14. The electrolytic composite polishing method according to claim 10, wherein the polishing is performed while measuring the residual film thickness of the conductive film by an eddy current method. 15. The electrolytic composite polishing method according to claim 10, wherein the conductive film is a town film. 59 320663 200936309 16. An electrolytic composite polishing method in which a surface of the substrate is pressed to a predetermined contact surface pressure by bringing an electrolytic solution into contact with a metal film formed on a surface of the substrate and applying a voltage to the metal film. An electrolytic composite polishing method for polishing a surface of the metal film while the substrate is simultaneously moved relative to the polishing pad, wherein the electrolyte solution is a pH 4 to 10, and the metal film is a lower layer film and a resistor. The electrolytic composite polishing method comprises: a step of disposing the voltage application point on a peripheral portion of the substrate, and removing the conductive film on the peripheral portion to expose the base film. And a step of moving the application point of the voltage from the peripheral edge portion of the substrate to the central portion to expose the base film after the process. 17. An electrolytic composite polishing method in which a surface of the substrate is pressed to a polishing pad at a predetermined contact surface pressure while contacting an electrolytic solution with a metal film formed on a surface of the substrate and applying a voltage to the metal film. An electrolytic composite polishing method for polishing a surface of the metal film by relatively moving the substrate and the polishing pad, wherein the electrolyte solution has a pH of 4 to 10, and the metal film is composed of a lower layer of a base film and a resistor. a method of forming a conductive film having a small upper layer, wherein the electrolytic composite polishing method includes: a step of disposing the voltage application point on a peripheral portion of the substrate, and first removing the conductive film on the peripheral portion to expose the base film; Then, the step of increasing the voltage is performed by moving the application point of the voltage from the peripheral portion of the substrate 60 320663 200936309 toward the center portion to expose the base film, and the step of increasing the voltage after the base film is exposed or exposed. System: in order to move the aforementioned substrate and the aforementioned polishing pad while pressing the contact surface into a 〇 Temporal increase the voltage, current density increases from the converted voltage decreases as the threshold voltage, the voltage is increased to the base film so that the exposed area exceeds the voltage threshold voltage. 18. The electrolytic composite polishing method according to claim 1 or 2, wherein the voltage applied to the conductive film is a positive voltage. 19. The polishing method of claim 7, wherein the voltage applied to the conductive film is a positive voltage. 61 320663
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